Canonical Allele Identifier: CA1140030883
Gene: CASP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15525539C= , CM000663.2:g.15525539C= GRCh38
NC_000001.10:g.15852034C= , CM000663.1:g.15852034C= GRCh37
NC_000001.9:g.15724621C= NCBI36
NG_029188.1:g.4252G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000469637.1:c.-239+652G= ENSP00000480785.1:n.-239+652G=
XM_011542272.1:c.-118+652G= XP_011540574.1:n.-118+652G=