Canonical Allele Identifier: CA1041231202
Gene: CASP8 HGNC NCBI

Linked Data

dbSNP Id: rs1949620329
gnomAD v3: 2-201287836-T-C
gnomAD v4: 2-201287836-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201287836T>C , CM000664.2:g.201287836T>C GRCh38
NC_000002.11:g.202152559T>C , CM000664.1:g.202152559T>C GRCh37
NC_000002.10:g.201860804T>C NCBI36
NG_007497.1:g.59379T>C , LRG_34:g.59379T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000696069.1:c.1259+2519T>C ENSP00000512371.1:n.1259+2519T>C
Search 100 bp 5'
Search 100 bp 3'