Canonical Allele Identifier: CA832742487

Gene:

Linked Data

• dbSNP Id: rs1317341640
• MyVariant Identifiers: chr7:g.123946368A>G (hg19) ; chr7:g.124306314A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.124306314A>G , CM000669.2:g.124306314A>G	GRCh38
NC_000007.13:g.123946368A>G , CM000669.1:g.123946368A>G	GRCh37
NC_000007.12:g.123733604A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_002956584.1:n.73-164A>G