Canonical Allele Identifier: CA851031746

Gene:

Linked Data

• dbSNP Id: rs1457833453
• gnomAD v3: 8-33808352-G-T
• gnomAD v4: 8-33808352-G-T
• MyVariant Identifiers: chr8:g.33665870G>T (hg19) ; chr8:g.33808352G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.33808352G>T , CM000670.2:g.33808352G>T	GRCh38
NC_000008.10:g.33665870G>T , CM000670.1:g.33665870G>T	GRCh37
NC_000008.9:g.33785412G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_949659.1:n.240+11916G>T
XR_002956701.1:n.240+11916G>T