Canonical Allele Identifier:
CA1233224692
Gene:
Linked Data
dbSNP Id:
rs1661039078
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.773351G>T , CM000664.2:g.773351G>T | GRCh38 |
| NC_000002.11:g.773351G>T , CM000664.1:g.773351G>T | GRCh37 |
| NC_000002.10:g.763351G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011510439.1:c.-24-3485G>T | XP_011508741.1:n.-24-3485G>T | |
| XM_011510440.1:c.-24-3485G>T | XP_011508742.1:n.-24-3485G>T | |
| XM_011510441.1:c.-24-3485G>T | XP_011508743.1:n.-24-3485G>T | |
| XM_011510442.1:c.-24-3485G>T | XP_011508744.1:n.-24-3485G>T | |
| XM_011510443.1:c.-24-3485G>T | XP_011508745.1:n.-24-3485G>T | |
| XR_922708.1:n.4001-3485G>T |