Canonical Allele Identifier: CA2662639078
Gene: CASP8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201287862del , CM000664.2:g.201287862del GRCh38
NC_000002.11:g.202152585del , CM000664.1:g.202152585del GRCh37
NC_000002.10:g.201860830del NCBI36
NG_007497.1:g.59405del , LRG_34:g.59405del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696069.1:c.1259+2545del ENSP00000512371.1:n.1259+2545del