Canonical Allele Identifier: CA584987412

Gene:

Linked Data

• dbSNP Id: rs1426437603
• gnomAD v2: 8-126486431-T-A
• gnomAD v3: 8-125474189-T-A
• gnomAD v4: 8-125474189-T-A
• MyVariant Identifiers: chr8:g.126486431T>A (hg19) ; chr8:g.125474189T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.125474189T>A , CM000670.2:g.125474189T>A	GRCh38
NC_000008.10:g.126486431T>A , CM000670.1:g.126486431T>A	GRCh37
NC_000008.9:g.126555613T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_928628.1:n.256+875T>A