Canonical Allele Identifier: CA2753865067
Gene: CASP8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201287749G>C , CM000664.2:g.201287749G>C GRCh38
NC_000002.11:g.202152472G>C , CM000664.1:g.202152472G>C GRCh37
NC_000002.10:g.201860717G>C NCBI36
NG_007497.1:g.59292G>C , LRG_34:g.59292G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000696069.1:c.1259+2432G>C ENSP00000512371.1:n.1259+2432G>C