Canonical Allele Identifier: CA1320996850
Gene: CASP8 HGNC NCBI

Linked Data

dbSNP Id: rs1559379226
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201287999C>A , CM000664.2:g.201287999C>A GRCh38
NC_000002.11:g.202152722C>A , CM000664.1:g.202152722C>A GRCh37
NC_000002.10:g.201860967C>A NCBI36
NG_007497.1:g.59542C>A , LRG_34:g.59542C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696069.1:c.1259+2682C>A ENSP00000512371.1:n.1259+2682C>A
Search 100 bp 5'
Search 100 bp 3'