Canonical Allele Identifier: CA1320996745
Gene: CASP8 HGNC NCBI

Linked Data

dbSNP Id: rs1949617703

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201287754T>G , CM000664.2:g.201287754T>G GRCh38
NC_000002.11:g.202152477T>G , CM000664.1:g.202152477T>G GRCh37
NC_000002.10:g.201860722T>G NCBI36
NG_007497.1:g.59297T>G , LRG_34:g.59297T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696069.1:c.1259+2437T>G ENSP00000512371.1:n.1259+2437T>G