Canonical Allele Identifier: CA1320996862
Gene: CASP8 HGNC NCBI

Linked Data

dbSNP Id: rs1576398626
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201288032G>T , CM000664.2:g.201288032G>T GRCh38
NC_000002.11:g.202152755G>T , CM000664.1:g.202152755G>T GRCh37
NC_000002.10:g.201861000G>T NCBI36
NG_007497.1:g.59575G>T , LRG_34:g.59575G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696069.1:c.1259+2715G>T ENSP00000512371.1:n.1259+2715G>T
Search 100 bp 5'
Search 100 bp 3'