Canonical Allele Identifier: CA1320996841
Gene: CASP8 HGNC NCBI

Linked Data

dbSNP Id: rs1949624901

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201287977_201287978dup , CM000664.2:g.201287977_201287978dup GRCh38
NC_000002.11:g.202152700_202152701dup , CM000664.1:g.202152700_202152701dup GRCh37
NC_000002.10:g.201860945_201860946dup NCBI36
NG_007497.1:g.59520_59521dup , LRG_34:g.59520_59521dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000696069.1:c.1259+2660_1259+2661dup ENSP00000512371.1:n.1259+2660_1259+2661dup