Canonical Allele Identifier: CA855697523

Gene:

Linked Data

• dbSNP Id: rs1188033695
• gnomAD v3: 8-79191155-A-C
• gnomAD v4: 8-79191155-A-C
• MyVariant Identifiers: chr8:g.80103390A>C (hg19) ; chr8:g.79191155A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.79191155A>C , CM000670.2:g.79191155A>C	GRCh38
NC_000008.10:g.80103390A>C , CM000670.1:g.80103390A>C	GRCh37
NC_000008.9:g.80265945A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001745720.1:n.105+784A>C