Canonical Allele Identifier: CA763326506
Gene: CASP8 HGNC NCBI

Linked Data

dbSNP Id: rs1387430468
MyVariant Identifiers: chr2:g.202152443G>A (hg19) chr2:g.201287720G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201287720G>A , CM000664.2:g.201287720G>A GRCh38
NC_000002.11:g.202152443G>A , CM000664.1:g.202152443G>A GRCh37
NC_000002.10:g.201860688G>A NCBI36
NG_007497.1:g.59263G>A , LRG_34:g.59263G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696069.1:c.1259+2403G>A ENSP00000512371.1:n.1259+2403G>A
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