Canonical Allele Identifier: CA1041231174
Gene: CASP8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201287737G>T , CM000664.2:g.201287737G>T GRCh38
NC_000002.11:g.202152460G>T , CM000664.1:g.202152460G>T GRCh37
NC_000002.10:g.201860705G>T NCBI36
NG_007497.1:g.59280G>T , LRG_34:g.59280G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696069.1:c.1259+2420G>T ENSP00000512371.1:n.1259+2420G>T