Canonical Allele Identifier: CA93117929
Gene:

Linked Data

dbSNP Id: rs981251376

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578317G>A , CM000666.2:g.12578317G>A GRCh38
NC_000004.11:g.12579941G>A , CM000666.1:g.12579941G>A GRCh37
NC_000004.10:g.12189039G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31025C>T
XR_001741374.1:n.254+44338C>T
XR_925406.3:n.140+31025C>T