Canonical Allele Identifier: CA763326569
Gene: CASP8 HGNC NCBI

Linked Data

dbSNP Id: rs1481497278
gnomAD v3: 2-201288015-G-A
gnomAD v4: 2-201288015-G-A
MyVariant Identifiers: chr2:g.202152738G>A (hg19) chr2:g.201288015G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201288015G>A , CM000664.2:g.201288015G>A GRCh38
NC_000002.11:g.202152738G>A , CM000664.1:g.202152738G>A GRCh37
NC_000002.10:g.201860983G>A NCBI36
NG_007497.1:g.59558G>A , LRG_34:g.59558G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696069.1:c.1259+2698G>A ENSP00000512371.1:n.1259+2698G>A
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