Canonical Allele Identifier: CA1258276517
Gene:

Linked Data

dbSNP Id: rs1672710607

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.67637475T>C , CM000664.2:g.67637475T>C GRCh38
NC_000002.11:g.67864607T>C , CM000664.1:g.67864607T>C GRCh37
NC_000002.10:g.67718111T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739524.1:n.65+13491A>G