Canonical Allele Identifier: CA89721265

Gene:

Linked Data

• dbSNP Id: rs765000652
• gnomAD v3: 3-190286424-A-G
• gnomAD v4: 3-190286424-A-G
• MyVariant Identifiers: chr3:g.190004213A>G (hg19) ; chr3:g.190286424A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190286424A>G , CM000665.2:g.190286424A>G	GRCh38
NC_000003.11:g.190004213A>G , CM000665.1:g.190004213A>G	GRCh37
NC_000003.10:g.191486907A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001741069.1:n.89-4054A>G