Canonical Allele Identifier: CA2753865076
Gene: CASP8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201288010G>T , CM000664.2:g.201288010G>T GRCh38
NC_000002.11:g.202152733G>T , CM000664.1:g.202152733G>T GRCh37
NC_000002.10:g.201860978G>T NCBI36
NG_007497.1:g.59553G>T , LRG_34:g.59553G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696069.1:c.1259+2693G>T ENSP00000512371.1:n.1259+2693G>T