Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs762557057
- Species
- Homo sapiens
- Symbol
- rs762557057
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ATRAID
- Location
- 2:27212295
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000002.12:g.27212295G>C
- HGVS.c name
- ENSEMBL:ENST00000380171.9:c.-74G>C
- ENSEMBL:ENST00000428518.5:c.-334-149C>G
- HGVS.p name
- ENSP00000484228:p.Arg31Thr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:27212041...27217183 (5.14 kb)
- Assembly version
- Not Available
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