Canonical Allele Identifier: CA763326573
Gene: CASP8 HGNC NCBI

Linked Data

dbSNP Id: rs1269698651
MyVariant Identifiers: chr2:g.202152740C>T (hg19) chr2:g.201288017C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201288017C>T , CM000664.2:g.201288017C>T GRCh38
NC_000002.11:g.202152740C>T , CM000664.1:g.202152740C>T GRCh37
NC_000002.10:g.201860985C>T NCBI36
NG_007497.1:g.59560C>T , LRG_34:g.59560C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696069.1:c.1259+2700C>T ENSP00000512371.1:n.1259+2700C>T
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