Canonical Allele Identifier: CA2753865069
Gene: CASP8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201287829T>C , CM000664.2:g.201287829T>C GRCh38
NC_000002.11:g.202152552T>C , CM000664.1:g.202152552T>C GRCh37
NC_000002.10:g.201860797T>C NCBI36
NG_007497.1:g.59372T>C , LRG_34:g.59372T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000696069.1:c.1259+2512T>C ENSP00000512371.1:n.1259+2512T>C