Canonical Allele Identifier: CA1320996847

Gene: CASP8

Linked Data

• dbSNP Id: rs1173031127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201287996A>C , CM000664.2:g.201287996A>C	GRCh38
NC_000002.11:g.202152719A>C , CM000664.1:g.202152719A>C	GRCh37
NC_000002.10:g.201860964A>C	NCBI36
NG_007497.1:g.59539A>C , LRG_34:g.59539A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696069.1:c.1259+2679A>C	ENSP00000512371.1:n.1259+2679A>C