Canonical Allele Identifier: CA2319713367
Gene: KDM4B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.5022529A= , CM000681.2:g.5022529A= GRCh38
NC_000019.9:g.5022540A= , CM000681.1:g.5022540A= GRCh37
NC_000019.8:g.4973540A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000159111.9:c.-26+6190A= MANE Select ENSP00000159111.3:n.-26+6190A=
ENST00000159111.8:c.-26+6190A= ENSP00000159111.3:n.-26+6190A=
ENST00000381759.8:c.-26+6190A= ENSP00000371178.3:n.-26+6190A=
ENST00000536461.5:c.-26+6190A= ENSP00000440495.1:n.-26+6190A=
ENST00000588337.5:c.-25-10337A= ENSP00000468514.1:n.-25-10337A=
ENST00000611640.4:c.-26+6190A= ENSP00000480642.1:n.-26+6190A=
NM_015015.2:c.-26+6190A= NP_055830.1:n.-26+6190A=
XM_005259521.2:c.-26+6190A= XP_005259578.2:n.-26+6190A=
XM_011527814.1:c.-136+6190A= XP_011526116.1:n.-136+6190A=
XM_011527815.1:c.-26+6190A= XP_011526117.1:n.-26+6190A=
XM_011527818.1:c.-26+6190A= XP_011526120.1:n.-26+6190A=
XM_011527819.1:c.-26+6190A= XP_011526121.1:n.-26+6190A=
XM_011527820.1:c.-26+6190A= XP_011526122.1:n.-26+6190A=
XM_011527821.1:c.-26+6190A= XP_011526123.1:n.-26+6190A=
XM_011527822.1:c.-26+6190A= XP_011526124.1:n.-26+6190A=
XR_936167.1:n.202+6190A=
XM_005259521.4:c.-26+6190A= XP_005259578.2:n.-26+6190A=
XM_011527814.2:c.-136+6190A= XP_011526116.1:n.-136+6190A=
XM_011527818.3:c.-26+6190A= XP_011526120.1:n.-26+6190A=
XM_011527819.2:c.-26+6190A= XP_011526121.1:n.-26+6190A=
XM_011527820.2:c.-26+6190A= XP_011526122.1:n.-26+6190A=
XM_011527821.2:c.-26+6190A= XP_011526123.1:n.-26+6190A=
XM_011527822.2:c.-26+6190A= XP_011526124.1:n.-26+6190A=
XM_017026503.1:c.-26+6190A= XP_016881992.1:n.-26+6190A=
XM_017026504.2:c.-26+6190A= XP_016881993.1:n.-26+6190A=
XM_017026505.2:c.-26+6190A= XP_016881994.1:n.-26+6190A=
XR_936167.2:n.227+6190A=
NM_015015.3:c.-26+6190A= MANE Select NP_055830.1:n.-26+6190A=
NM_001370093.1:c.-26+6190A= NP_001357022.1:n.-26+6190A=
NM_001370094.1:c.-26+6190A= NP_001357023.1:n.-26+6190A=