Canonical Allele Identifier: CA1320996818
Gene: CASP8 HGNC NCBI

Linked Data

dbSNP Id: rs1949623198

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201287914_201287917dup , CM000664.2:g.201287914_201287917dup GRCh38
NC_000002.11:g.202152637_202152640dup , CM000664.1:g.202152637_202152640dup GRCh37
NC_000002.10:g.201860882_201860885dup NCBI36
NG_007497.1:g.59457_59460dup , LRG_34:g.59457_59460dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000696069.1:c.1259+2597_1259+2600dup ENSP00000512371.1:n.1259+2597_1259+2600dup