Canonical Allele Identifier: CA168427895
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs10487524

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.145144438G>A , CM000669.2:g.145144438G>A GRCh38
NC_000007.13:g.144841531G>A , CM000669.1:g.144841531G>A GRCh37
NC_000007.12:g.144472464G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928090.1:n.1968-12497G>A
XR_928090.2:n.4143-12497G>A