Canonical Allele Identifier: CA905231325

Gene:

Linked Data

• dbSNP Id: rs1329490834
• MyVariant Identifiers: chr3:g.21248721G>A (hg19) ; chr3:g.21207229G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.21207229G>A , CM000665.2:g.21207229G>A	GRCh38
NC_000003.11:g.21248721G>A , CM000665.1:g.21248721G>A	GRCh37
NC_000003.10:g.21223725G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940646.1:n.254-3769G>A
XR_940646.2:n.547-3769G>A