Canonical Allele Identifier: CA904086773

Gene:

Linked Data

• dbSNP Id: rs1165963583
• MyVariant Identifiers: chr3:g.187649381T>A (hg19) ; chr3:g.187931593T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.187931593T>A , CM000665.2:g.187931593T>A	GRCh38
NC_000003.11:g.187649381T>A , CM000665.1:g.187649381T>A	GRCh37
NC_000003.10:g.189132075T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_924814.1:n.1321A>T