Canonical Allele Identifier: CA1140030880
Gene: CASP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15524988G= , CM000663.2:g.15524988G= GRCh38
NC_000001.10:g.15851483G= , CM000663.1:g.15851483G= GRCh37
NC_000001.9:g.15724070G= NCBI36
NG_029188.1:g.4803C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000469637.1:c.-239+1203C= ENSP00000480785.1:n.-239+1203C=
XM_011542272.1:c.-118+1203C= XP_011540574.1:n.-118+1203C=