Canonical Allele Identifier: CA682822635

Gene:

Linked Data

• dbSNP Id: rs1318089632
• MyVariant Identifiers: chr12:g.102895169A>G (hg19) ; chr12:g.102501391A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102501391A>G , CM000674.2:g.102501391A>G	GRCh38
NC_000012.11:g.102895169A>G , CM000674.1:g.102895169A>G	GRCh37
NC_000012.10:g.101419299A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001749289.1:n.1952+17503A>G