Canonical Allele Identifier: CA682822670

Gene:

Linked Data

• dbSNP Id: rs1469511095
• MyVariant Identifiers: chr12:g.102895279G>A (hg19) ; chr12:g.102501501G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102501501G>A , CM000674.2:g.102501501G>A	GRCh38
NC_000012.11:g.102895279G>A , CM000674.1:g.102895279G>A	GRCh37
NC_000012.10:g.101419409G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001749289.1:n.1952+17613G>A