Canonical Allele Identifier: CA1320996854

Gene: CASP8

Linked Data

• dbSNP Id: rs1949625996

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201288012T>C , CM000664.2:g.201288012T>C	GRCh38
NC_000002.11:g.202152735T>C , CM000664.1:g.202152735T>C	GRCh37
NC_000002.10:g.201860980T>C	NCBI36
NG_007497.1:g.59555T>C , LRG_34:g.59555T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696069.1:c.1259+2695T>C	ENSP00000512371.1:n.1259+2695T>C