Canonical Allele Identifier: CA1740470101
Gene:

Linked Data

dbSNP Id: rs1795645844

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.124306301T>C , CM000669.2:g.124306301T>C GRCh38
NC_000007.13:g.123946355T>C , CM000669.1:g.123946355T>C GRCh37
NC_000007.12:g.123733591T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_002956584.1:n.73-177T>C