Canonical Allele Identifier: CA63898513
Gene: CASP8 HGNC NCBI

Linked Data

dbSNP Id: rs533766190
gnomAD v4: 2-201287845-G-T
MyVariant Identifiers: chr2:g.202152568G>T (hg19) chr2:g.201287845G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201287845G>T , CM000664.2:g.201287845G>T GRCh38
NC_000002.11:g.202152568G>T , CM000664.1:g.202152568G>T GRCh37
NC_000002.10:g.201860813G>T NCBI36
NG_007497.1:g.59388G>T , LRG_34:g.59388G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000696069.1:c.1259+2528G>T ENSP00000512371.1:n.1259+2528G>T
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