Canonical Allele Identifier: CA846955657

Gene:

Linked Data

• dbSNP Id: rs1486986816
• gnomAD v3: 8-125474244-A-C
• gnomAD v4: 8-125474244-A-C
• MyVariant Identifiers: chr8:g.126486486A>C (hg19) ; chr8:g.125474244A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.125474244A>C , CM000670.2:g.125474244A>C	GRCh38
NC_000008.10:g.126486486A>C , CM000670.1:g.126486486A>C	GRCh37
NC_000008.9:g.126555668A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_928628.1:n.256+930A>C