Canonical Allele Identifier: CA1320996828
Gene: CASP8 HGNC NCBI

Linked Data

dbSNP Id: rs963195822

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201287934T>C , CM000664.2:g.201287934T>C GRCh38
NC_000002.11:g.202152657T>C , CM000664.1:g.202152657T>C GRCh37
NC_000002.10:g.201860902T>C NCBI36
NG_007497.1:g.59477T>C , LRG_34:g.59477T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696069.1:c.1259+2617T>C ENSP00000512371.1:n.1259+2617T>C