Canonical Allele Identifier: CA2662639066
Gene: CASP8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201287790C>A , CM000664.2:g.201287790C>A GRCh38
NC_000002.11:g.202152513C>A , CM000664.1:g.202152513C>A GRCh37
NC_000002.10:g.201860758C>A NCBI36
NG_007497.1:g.59333C>A , LRG_34:g.59333C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696069.1:c.1259+2473C>A ENSP00000512371.1:n.1259+2473C>A