Canonical Allele Identifier: CA184586830

Gene:

Linked Data

• dbSNP Id: rs960694114
• gnomAD v3: 8-123753545-G-A
• gnomAD v4: 8-123753545-G-A
• MyVariant Identifiers: chr8:g.124765785G>A (hg19) ; chr8:g.123753545G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.123753545G>A , CM000670.2:g.123753545G>A	GRCh38
NC_000008.10:g.124765785G>A , CM000670.1:g.124765785G>A	GRCh37
NC_000008.9:g.124834966G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_928607.1:n.153-11238G>A
XR_928607.3:n.324-11238G>A