Canonical Allele Identifier: CA1320996860

Gene: CASP8

Linked Data

• dbSNP Id: rs1576398617

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201288031A>G , CM000664.2:g.201288031A>G	GRCh38
NC_000002.11:g.202152754A>G , CM000664.1:g.202152754A>G	GRCh37
NC_000002.10:g.201860999A>G	NCBI36
NG_007497.1:g.59574A>G , LRG_34:g.59574A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696069.1:c.1259+2714A>G	ENSP00000512371.1:n.1259+2714A>G