Canonical Allele Identifier: CA889649180
Gene: CASP9 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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