Canonical Allele Identifier: CA1320996829
Gene: CASP8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201287934T= , CM000664.2:g.201287934T= GRCh38
NC_000002.11:g.202152657T= , CM000664.1:g.202152657T= GRCh37
NC_000002.10:g.201860902T= NCBI36
NG_007497.1:g.59477T= , LRG_34:g.59477T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696069.1:c.1259+2617T= ENSP00000512371.1:n.1259+2617T=