Canonical Allele Identifier: CA1320996819
Gene: CASP8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201287914A= , CM000664.2:g.201287914A= GRCh38
NC_000002.11:g.202152637A= , CM000664.1:g.202152637A= GRCh37
NC_000002.10:g.201860882A= NCBI36
NG_007497.1:g.59457A= , LRG_34:g.59457A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696069.1:c.1259+2597A= ENSP00000512371.1:n.1259+2597A=