Canonical Allele Identifier: CA1041231239
Gene: CASP8 HGNC NCBI

Linked Data

dbSNP Id: rs1274869590
gnomAD v3: 2-201287914-A-C
gnomAD v4: 2-201287914-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201287914A>C , CM000664.2:g.201287914A>C GRCh38
NC_000002.11:g.202152637A>C , CM000664.1:g.202152637A>C GRCh37
NC_000002.10:g.201860882A>C NCBI36
NG_007497.1:g.59457A>C , LRG_34:g.59457A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696069.1:c.1259+2597A>C ENSP00000512371.1:n.1259+2597A>C
Search 100 bp 5'
Search 100 bp 3'