Canonical Allele Identifier: CA14724519
Gene: KDM4B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs263063

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.5022593T>C , CM000681.2:g.5022593T>C GRCh38
NC_000019.9:g.5022604T>C , CM000681.1:g.5022604T>C GRCh37
NC_000019.8:g.4973604T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_015015.2:c.-26+6254T>C VV NP_055830.1:p.=
XM_005259521.2:c.-26+6254T>C XP_005259578.2:p.=
XM_011527814.1:c.-136+6254T>C XP_011526116.1:p.=
XM_011527815.1:c.-26+6254T>C XP_011526117.1:p.=
XM_011527818.1:c.-26+6254T>C XP_011526120.1:p.=
XM_011527819.1:c.-26+6254T>C XP_011526121.1:p.=
XM_011527820.1:c.-26+6254T>C XP_011526122.1:p.=
XM_011527821.1:c.-26+6254T>C XP_011526123.1:p.=
XM_011527822.1:c.-26+6254T>C XP_011526124.1:p.=
XR_936167.1:n.202+6254T>C
XM_005259521.4:c.-26+6254T>C XP_005259578.2:p.=
XM_011527814.2:c.-136+6254T>C XP_011526116.1:p.=
XM_011527818.3:c.-26+6254T>C XP_011526120.1:p.=
XM_011527819.2:c.-26+6254T>C XP_011526121.1:p.=
XM_011527820.2:c.-26+6254T>C XP_011526122.1:p.=
XM_011527821.2:c.-26+6254T>C XP_011526123.1:p.=
XM_011527822.2:c.-26+6254T>C XP_011526124.1:p.=
XM_017026503.1:c.-26+6254T>C XP_016881992.1:p.=
XM_017026504.2:c.-26+6254T>C XP_016881993.1:p.=
XM_017026505.2:c.-26+6254T>C XP_016881994.1:p.=
XR_936167.2:n.227+6254T>C
NM_015015.3:c.-26+6254T>C VV MANE Preferred NP_055830.1:p.=
ENST00000159111.8:c.-26+6254T>C ENSP00000159111.3:p.=
ENST00000381759.8:c.-26+6254T>C ENSP00000371178.3:p.=
ENST00000536461.5:c.-26+6254T>C ENSP00000440495.1:p.=
ENST00000588337.5:c.-25-10273T>C ENSP00000468514.1:p.=
ENST00000611640.4:c.-26+6254T>C ENSP00000480642.1:p.=