Canonical Allele Identifier: CA1284673938
Gene:

Linked Data

dbSNP Id: rs1573478906

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122883773T>G , CM000664.2:g.122883773T>G GRCh38
NC_000002.11:g.123641349T>G , CM000664.1:g.123641349T>G GRCh37
NC_000002.10:g.123357819T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923292.1:n.1125-1169T>G
XR_001739692.1:n.1451-1169T>G
XR_923292.2:n.1358-1169T>G