Canonical Allele Identifier: CA763326535

Gene: CASP8

Linked Data

• dbSNP Id: rs1368065001
• MyVariant Identifiers: chr2:g.202152554T>C (hg19) ; chr2:g.201287831T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201287831T>C , CM000664.2:g.201287831T>C	GRCh38
NC_000002.11:g.202152554T>C , CM000664.1:g.202152554T>C	GRCh37
NC_000002.10:g.201860799T>C	NCBI36
NG_007497.1:g.59374T>C , LRG_34:g.59374T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696069.1:c.1259+2514T>C	ENSP00000512371.1:n.1259+2514T>C