Canonical Allele Identifier: CA851031680

Gene:

Linked Data

• dbSNP Id: rs1458766579
• gnomAD v3: 8-33808229-A-G
• gnomAD v4: 8-33808229-A-G
• MyVariant Identifiers: chr8:g.33665747A>G (hg19) ; chr8:g.33808229A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.33808229A>G , CM000670.2:g.33808229A>G	GRCh38
NC_000008.10:g.33665747A>G , CM000670.1:g.33665747A>G	GRCh37
NC_000008.9:g.33785289A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_949659.1:n.240+11793A>G
XR_002956701.1:n.240+11793A>G