Canonical Allele Identifier: CA906943506

Gene:

Linked Data

• dbSNP Id: rs1482588382
• gnomAD v3: 3-39263210-G-T
• gnomAD v4: 3-39263210-G-T
• MyVariant Identifiers: chr3:g.39304701G>T (hg19) ; chr3:g.39263210G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39263210G>T , CM000665.2:g.39263210G>T	GRCh38
NC_000003.11:g.39304701G>T , CM000665.1:g.39304701G>T	GRCh37
NC_000003.10:g.39279705G>T	NCBI36
NG_016362.1:g.23526C>A

Transcript Alleles

HGVS	Amino-acid change
XR_001740660.2:n.2727G>T