Canonical Allele Identifier: CA81296270

Gene:

Linked Data

• dbSNP Id: rs970985703
• MyVariant Identifiers: chr3:g.109462357T>C (hg19) ; chr3:g.109743510T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.109743510T>C , CM000665.2:g.109743510T>C	GRCh38
NC_000003.11:g.109462357T>C , CM000665.1:g.109462357T>C	GRCh37
NC_000003.10:g.110945047T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_924325.1:n.142+63315T>C