Canonical Allele Identifier: CA166591540

Gene:

Linked Data

• dbSNP Id: rs956236610
• MyVariant Identifiers: chr7:g.123946374A>G (hg19) ; chr7:g.124306320A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.124306320A>G , CM000669.2:g.124306320A>G	GRCh38
NC_000007.13:g.123946374A>G , CM000669.1:g.123946374A>G	GRCh37
NC_000007.12:g.123733610A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_002956584.1:n.73-158A>G