Canonical Allele Identifier:
CA10995425
Gene:
Linked Data
dbSNP Id:
rs4380275
gnomAD v2:
2-773278-C-T
gnomAD v3:
2-773278-C-T
gnomAD v4:
2-773278-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.773278C>T , CM000664.2:g.773278C>T | GRCh38 |
| NC_000002.11:g.773278C>T , CM000664.1:g.773278C>T | GRCh37 |
| NC_000002.10:g.763278C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XM_011510439.1:c.-24-3558C>T | XP_011508741.1:n.-24-3558C>T | |
| XM_011510440.1:c.-24-3558C>T | XP_011508742.1:n.-24-3558C>T | |
| XM_011510441.1:c.-24-3558C>T | XP_011508743.1:n.-24-3558C>T | |
| XM_011510442.1:c.-24-3558C>T | XP_011508744.1:n.-24-3558C>T | |
| XM_011510443.1:c.-24-3558C>T | XP_011508745.1:n.-24-3558C>T | |
| XR_922708.1:n.4001-3558C>T |