Canonical Allele Identifier: CA63898581
Gene: CASP8 HGNC NCBI

Linked Data

dbSNP Id: rs1043342249
gnomAD v2: 2-202152757-C-T
gnomAD v3: 2-201288034-C-T
gnomAD v4: 2-201288034-C-T
MyVariant Identifiers: chr2:g.202152757C>T (hg19) chr2:g.201288034C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201288034C>T , CM000664.2:g.201288034C>T GRCh38
NC_000002.11:g.202152757C>T , CM000664.1:g.202152757C>T GRCh37
NC_000002.10:g.201861002C>T NCBI36
NG_007497.1:g.59577C>T , LRG_34:g.59577C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696069.1:c.1259+2717C>T ENSP00000512371.1:n.1259+2717C>T
Search 100 bp 5'
Search 100 bp 3'