Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs199846944
- Species
- Homo sapiens
- Symbol
- rs199846944
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ABCA12
- Location
- 2:214932707
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant&non coding transcript variant
- HGVS.g name
- (GRCh38)2:214932707T>C
- HGVS.c name
- ENSEMBL:ENST00000272895.12:c.7715A>G
- ENSEMBL:ENST00000389661.4:c.6761A>G
- HGVS.p name
- ENSP00000272895:p.Tyr2572Cys
- ENSP00000374312:p.Tyr2254Cys
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:214931542...215138626 (207.08 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction