Canonical Allele Identifier: CA63898576
Gene: CASP8 HGNC NCBI

Linked Data

dbSNP Id: rs992547041
gnomAD v2: 2-202152732-C-T
gnomAD v3: 2-201288009-C-T
gnomAD v4: 2-201288009-C-T
MyVariant Identifiers: chr2:g.202152732C>T (hg19) chr2:g.201288009C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201288009C>T , CM000664.2:g.201288009C>T GRCh38
NC_000002.11:g.202152732C>T , CM000664.1:g.202152732C>T GRCh37
NC_000002.10:g.201860977C>T NCBI36
NG_007497.1:g.59552C>T , LRG_34:g.59552C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696069.1:c.1259+2692C>T ENSP00000512371.1:n.1259+2692C>T
Search 100 bp 5'
Search 100 bp 3'