Canonical Allele Identifier: CA2519434865
Gene: CASP8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201287947C>T , CM000664.2:g.201287947C>T GRCh38
NC_000002.11:g.202152670C>T , CM000664.1:g.202152670C>T GRCh37
NC_000002.10:g.201860915C>T NCBI36
NG_007497.1:g.59490C>T , LRG_34:g.59490C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696069.1:c.1259+2630C>T ENSP00000512371.1:n.1259+2630C>T