Canonical Allele Identifier: CA2662639046

Gene: CASP8

Linked Data

• gnomAD v4: 2-201287738-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201287738T>C , CM000664.2:g.201287738T>C	GRCh38
NC_000002.11:g.202152461T>C , CM000664.1:g.202152461T>C	GRCh37
NC_000002.10:g.201860706T>C	NCBI36
NG_007497.1:g.59281T>C , LRG_34:g.59281T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000696069.1:c.1259+2421T>C	ENSP00000512371.1:n.1259+2421T>C