Canonical Allele Identifier: CA63898523
Gene: CASP8 HGNC NCBI

Linked Data

dbSNP Id: rs779134210

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201287878dup , CM000664.2:g.201287878dup GRCh38
NC_000002.11:g.202152601dup , CM000664.1:g.202152601dup GRCh37
NC_000002.10:g.201860846dup NCBI36
NG_007497.1:g.59421dup , LRG_34:g.59421dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000696069.1:c.1259+2561dup ENSP00000512371.1:n.1259+2561dup