Canonical Allele Identifier: CA904086772

Gene:

Linked Data

• dbSNP Id: rs1396904091
• gnomAD v3: 3-187931591-A-G
• gnomAD v4: 3-187931591-A-G
• MyVariant Identifiers: chr3:g.187649379A>G (hg19) ; chr3:g.187931591A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.187931591A>G , CM000665.2:g.187931591A>G	GRCh38
NC_000003.11:g.187649379A>G , CM000665.1:g.187649379A>G	GRCh37
NC_000003.10:g.189132073A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_924814.1:n.1323T>C