Canonical Allele Identifier: CA63898503

Gene: CASP8

Linked Data

• dbSNP Id: rs965743403
• gnomAD v3: 2-201287791-A-T
• gnomAD v4: 2-201287791-A-T
• MyVariant Identifiers: chr2:g.202152514A>T (hg19) ; chr2:g.201287791A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201287791A>T , CM000664.2:g.201287791A>T	GRCh38
NC_000002.11:g.202152514A>T , CM000664.1:g.202152514A>T	GRCh37
NC_000002.10:g.201860759A>T	NCBI36
NG_007497.1:g.59334A>T , LRG_34:g.59334A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000696069.1:c.1259+2474A>T	ENSP00000512371.1:n.1259+2474A>T