Canonical Allele Identifier: CA2542065200
Gene: CASP8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201287843T>C , CM000664.2:g.201287843T>C GRCh38
NC_000002.11:g.202152566T>C , CM000664.1:g.202152566T>C GRCh37
NC_000002.10:g.201860811T>C NCBI36
NG_007497.1:g.59386T>C , LRG_34:g.59386T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696069.1:c.1259+2526T>C ENSP00000512371.1:n.1259+2526T>C