Canonical Allele Identifier: CA2662639072
Gene: CASP8 HGNC NCBI

Linked Data

gnomAD v4: 2-201287832-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201287832A>G , CM000664.2:g.201287832A>G GRCh38
NC_000002.11:g.202152555A>G , CM000664.1:g.202152555A>G GRCh37
NC_000002.10:g.201860800A>G NCBI36
NG_007497.1:g.59375A>G , LRG_34:g.59375A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000696069.1:c.1259+2515A>G ENSP00000512371.1:n.1259+2515A>G
Search 100 bp 5'
Search 100 bp 3'