Canonical Allele Identifier: CA1017110262
Gene: AHCY HGNC NCBI

Linked Data

dbSNP Id: rs1568781202

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.34280222T>C , CM000682.2:g.34280222T>C GRCh38
NC_000020.10:g.32868028T>C , CM000682.1:g.32868028T>C GRCh37
NC_000020.9:g.32331689T>C NCBI36
NG_012630.1:g.36581A>G
NG_012630.2:g.36581A>G

Transcript Alleles

HGVS Amino-acid Change
XM_011528657.1:c.*7+805A>G XP_011526959.1:n.*7+805A>G
XM_011528658.1:c.*7+805A>G XP_011526960.1:n.*7+805A>G
XM_011528657.2:c.*7+805A>G XP_011526959.2:n.*7+805A>G
XM_011528658.3:c.*7+805A>G XP_011526960.2:n.*7+805A>G
XM_017027709.2:c.*7+805A>G XP_016883198.1:n.*7+805A>G