Canonical Allele Identifier: CA538932903

Gene: CASP8

Linked Data

• dbSNP Id: rs1273128049
• gnomAD v2: 2-202152704-A-G
• gnomAD v3: 2-201287981-A-G
• gnomAD v4: 2-201287981-A-G
• MyVariant Identifiers: chr2:g.202152704A>G (hg19) ; chr2:g.201287981A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201287981A>G , CM000664.2:g.201287981A>G	GRCh38
NC_000002.11:g.202152704A>G , CM000664.1:g.202152704A>G	GRCh37
NC_000002.10:g.201860949A>G	NCBI36
NG_007497.1:g.59524A>G , LRG_34:g.59524A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696069.1:c.1259+2664A>G	ENSP00000512371.1:n.1259+2664A>G