Canonical Allele Identifier: CA63898546
Gene: CASP8 HGNC NCBI

Linked Data

dbSNP Id: rs963195822
gnomAD v3: 2-201287934-T-G
gnomAD v4: 2-201287934-T-G
MyVariant Identifiers: chr2:g.202152657T>G (hg19) chr2:g.201287934T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201287934T>G , CM000664.2:g.201287934T>G GRCh38
NC_000002.11:g.202152657T>G , CM000664.1:g.202152657T>G GRCh37
NC_000002.10:g.201860902T>G NCBI36
NG_007497.1:g.59477T>G , LRG_34:g.59477T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696069.1:c.1259+2617T>G ENSP00000512371.1:n.1259+2617T>G
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