Canonical Allele Identifier: CA1320996839
Gene: CASP8 HGNC NCBI

Linked Data

dbSNP Id: rs1949624795

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201287974_201287976dup , CM000664.2:g.201287974_201287976dup GRCh38
NC_000002.11:g.202152697_202152699dup , CM000664.1:g.202152697_202152699dup GRCh37
NC_000002.10:g.201860942_201860944dup NCBI36
NG_007497.1:g.59517_59519dup , LRG_34:g.59517_59519dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000696069.1:c.1259+2657_1259+2659dup ENSP00000512371.1:n.1259+2657_1259+2659dup