Canonical Allele Identifier: CA63898593
Gene: CASP8 HGNC NCBI

Linked Data

dbSNP Id: rs904670555
gnomAD v3: 2-201288036-C-T
gnomAD v4: 2-201288036-C-T
MyVariant Identifiers: chr2:g.202152759C>T (hg19) chr2:g.201288036C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201288036C>T , CM000664.2:g.201288036C>T GRCh38
NC_000002.11:g.202152759C>T , CM000664.1:g.202152759C>T GRCh37
NC_000002.10:g.201861004C>T NCBI36
NG_007497.1:g.59579C>T , LRG_34:g.59579C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696069.1:c.1259+2719C>T ENSP00000512371.1:n.1259+2719C>T
Search 100 bp 5'
Search 100 bp 3'