Canonical Allele Identifier: CA2556351855
Gene: CASP8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201288013G>A , CM000664.2:g.201288013G>A GRCh38
NC_000002.11:g.202152736G>A , CM000664.1:g.202152736G>A GRCh37
NC_000002.10:g.201860981G>A NCBI36
NG_007497.1:g.59556G>A , LRG_34:g.59556G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696069.1:c.1259+2696G>A ENSP00000512371.1:n.1259+2696G>A