Canonical Allele Identifier: CA2662639053
Gene: CASP8 HGNC NCBI

Linked Data

gnomAD v4: 2-201287756-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201287756A>G , CM000664.2:g.201287756A>G GRCh38
NC_000002.11:g.202152479A>G , CM000664.1:g.202152479A>G GRCh37
NC_000002.10:g.201860724A>G NCBI36
NG_007497.1:g.59299A>G , LRG_34:g.59299A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696069.1:c.1259+2439A>G ENSP00000512371.1:n.1259+2439A>G
Search 100 bp 5'
Search 100 bp 3'