Canonical Allele Identifier: CA185510870

Gene:

Linked Data

• dbSNP Id: rs747255108
• gnomAD v3: 8-125478356-G-A
• gnomAD v4: 8-125478356-G-A
• MyVariant Identifiers: chr8:g.126490598G>A (hg19) ; chr8:g.125478356G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.125478356G>A , CM000670.2:g.125478356G>A	GRCh38
NC_000008.10:g.126490598G>A , CM000670.1:g.126490598G>A	GRCh37
NC_000008.9:g.126559780G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_928628.1:n.256+5042G>A