Canonical Allele Identifier: CA905231265

Gene:

Linked Data

• dbSNP Id: rs1441577305
• gnomAD v3: 3-21207106-A-G
• gnomAD v4: 3-21207106-A-G
• MyVariant Identifiers: chr3:g.21248598A>G (hg19) ; chr3:g.21207106A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.21207106A>G , CM000665.2:g.21207106A>G	GRCh38
NC_000003.11:g.21248598A>G , CM000665.1:g.21248598A>G	GRCh37
NC_000003.10:g.21223602A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940646.1:n.254-3892A>G
XR_940646.2:n.547-3892A>G