Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs149984222
- Species
- Homo sapiens
- Symbol
- rs149984222
- Category
- Variant
- Variant type
- SNP
- Overlaps
- BLOC1S5
- Location
- 6:8041235
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- non coding transcript exon variant
- HGVS.g name
- (GRCh38)6:8041235C>T
- HGVS.c name
- ENSEMBL:ENST00000244777.6:n.246G>A
- ENSEMBL:ENST00000397456.2:n.510G>A
- HGVS.p name
- ENSP00000380598:p.Glu77Lys
- NP_958437:p.Glu77Lys
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr6:8013567...8064414 (50.85 kb)
- Assembly version
- Not Available
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