Canonical Allele Identifier: CA905231317

Gene:

Linked Data

• dbSNP Id: rs1227351716
• MyVariant Identifiers: chr3:g.21248699C>G (hg19) ; chr3:g.21207207C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.21207207C>G , CM000665.2:g.21207207C>G	GRCh38
NC_000003.11:g.21248699C>G , CM000665.1:g.21248699C>G	GRCh37
NC_000003.10:g.21223703C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940646.1:n.254-3791C>G
XR_940646.2:n.547-3791C>G