Canonical Allele Identifier: CA583207375

Gene:

Linked Data

• dbSNP Id: rs1478030404
• gnomAD v2: 8-80103451-G-A
• gnomAD v3: 8-79191216-G-A
• gnomAD v4: 8-79191216-G-A
• MyVariant Identifiers: chr8:g.80103451G>A (hg19) ; chr8:g.79191216G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.79191216G>A , CM000670.2:g.79191216G>A	GRCh38
NC_000008.10:g.80103451G>A , CM000670.1:g.80103451G>A	GRCh37
NC_000008.9:g.80266006G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001745720.1:n.105+845G>A