Canonical Allele Identifier: CA63898572
Gene: CASP8 HGNC NCBI

Linked Data

dbSNP Id: rs938332543
gnomAD v3: 2-201287998-T-G
gnomAD v4: 2-201287998-T-G
MyVariant Identifiers: chr2:g.202152721T>G (hg19) chr2:g.201287998T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201287998T>G , CM000664.2:g.201287998T>G GRCh38
NC_000002.11:g.202152721T>G , CM000664.1:g.202152721T>G GRCh37
NC_000002.10:g.201860966T>G NCBI36
NG_007497.1:g.59541T>G , LRG_34:g.59541T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696069.1:c.1259+2681T>G ENSP00000512371.1:n.1259+2681T>G
Search 100 bp 5'
Search 100 bp 3'