Canonical Allele Identifier: CA1320996817
Gene: CASP8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201287911A= , CM000664.2:g.201287911A= GRCh38
NC_000002.11:g.202152634A= , CM000664.1:g.202152634A= GRCh37
NC_000002.10:g.201860879A= NCBI36
NG_007497.1:g.59454A= , LRG_34:g.59454A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696069.1:c.1259+2594A= ENSP00000512371.1:n.1259+2594A=