Canonical Allele Identifier: CA763326583
Gene: CASP8 HGNC NCBI

Linked Data

dbSNP Id: rs1487475060
gnomAD v3: 2-201288035-C-T
gnomAD v4: 2-201288035-C-T
MyVariant Identifiers: chr2:g.202152758C>T (hg19) chr2:g.201288035C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201288035C>T , CM000664.2:g.201288035C>T GRCh38
NC_000002.11:g.202152758C>T , CM000664.1:g.202152758C>T GRCh37
NC_000002.10:g.201861003C>T NCBI36
NG_007497.1:g.59578C>T , LRG_34:g.59578C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696069.1:c.1259+2718C>T ENSP00000512371.1:n.1259+2718C>T
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