Canonical Allele Identifier: CA1284673906
Gene:

Linked Data

dbSNP Id: rs1680369550

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122883740T>C , CM000664.2:g.122883740T>C GRCh38
NC_000002.11:g.123641316T>C , CM000664.1:g.123641316T>C GRCh37
NC_000002.10:g.123357786T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923292.1:n.1125-1202T>C
XR_001739692.1:n.1451-1202T>C
XR_923292.2:n.1358-1202T>C