Canonical Allele Identifier: CA763326558

Gene: CASP8

Linked Data

• dbSNP Id: rs1347937254
• MyVariant Identifiers: chr2:g.202152685C>T (hg19) ; chr2:g.201287962C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201287962C>T , CM000664.2:g.201287962C>T	GRCh38
NC_000002.11:g.202152685C>T , CM000664.1:g.202152685C>T	GRCh37
NC_000002.10:g.201860930C>T	NCBI36
NG_007497.1:g.59505C>T , LRG_34:g.59505C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696069.1:c.1259+2645C>T	ENSP00000512371.1:n.1259+2645C>T