Canonical Allele Identifier: CA763326554

Gene: CASP8

Linked Data

• dbSNP Id: rs1214742832
• MyVariant Identifiers: chr2:g.202152646T>G (hg19) ; chr2:g.201287923T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201287923T>G , CM000664.2:g.201287923T>G	GRCh38
NC_000002.11:g.202152646T>G , CM000664.1:g.202152646T>G	GRCh37
NC_000002.10:g.201860891T>G	NCBI36
NG_007497.1:g.59466T>G , LRG_34:g.59466T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696069.1:c.1259+2606T>G	ENSP00000512371.1:n.1259+2606T>G