Canonical Allele Identifier: CA63898561

Gene: CASP8

Linked Data

• dbSNP Id: rs927087276
• MyVariant Identifiers: chr2:g.202152675G>A (hg19) ; chr2:g.201287952G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201287952G>A , CM000664.2:g.201287952G>A	GRCh38
NC_000002.11:g.202152675G>A , CM000664.1:g.202152675G>A	GRCh37
NC_000002.10:g.201860920G>A	NCBI36
NG_007497.1:g.59495G>A , LRG_34:g.59495G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696069.1:c.1259+2635G>A	ENSP00000512371.1:n.1259+2635G>A