Canonical Allele Identifier: CA548664040

Gene:

Linked Data

• dbSNP Id: rs1405670684
• gnomAD v2: 3-187649360-A-G
• gnomAD v3: 3-187931572-A-G
• gnomAD v4: 3-187931572-A-G
• MyVariant Identifiers: chr3:g.187649360A>G (hg19) ; chr3:g.187931572A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.187931572A>G , CM000665.2:g.187931572A>G	GRCh38
NC_000003.11:g.187649360A>G , CM000665.1:g.187649360A>G	GRCh37
NC_000003.10:g.189132054A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_924814.1:n.1342T>C