Canonical Allele Identifier: CA763326563
Gene: CASP8 HGNC NCBI

Linked Data

dbSNP Id: rs1457856706
gnomAD v3: 2-201287964-CCTT-C
gnomAD v4: 2-201287964-CCTT-C
MyVariant Identifiers: chr2:g.202152688_202152690del (hg19) chr2:g.201287965_201287967del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201287969_201287971del , CM000664.2:g.201287969_201287971del GRCh38
NC_000002.11:g.202152692_202152694del , CM000664.1:g.202152692_202152694del GRCh37
NC_000002.10:g.201860937_201860939del NCBI36
NG_007497.1:g.59512_59514del , LRG_34:g.59512_59514del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696069.1:c.1259+2652_1259+2654del ENSP00000512371.1:n.1259+2652_1259+2654del
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