Canonical Allele Identifier: CA1320996820
Gene: CASP8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201287915T= , CM000664.2:g.201287915T= GRCh38
NC_000002.11:g.202152638T= , CM000664.1:g.202152638T= GRCh37
NC_000002.10:g.201860883T= NCBI36
NG_007497.1:g.59458T= , LRG_34:g.59458T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696069.1:c.1259+2598T= ENSP00000512371.1:n.1259+2598T=