Canonical Allele Identifier: CA2584575157
Gene: KMT2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35732491_35732493del , CM000681.2:g.35732491_35732493del GRCh38
NC_000019.9:g.36223392_36223394del , CM000681.1:g.36223392_36223394del GRCh37
NC_000019.8:g.40915232_40915234del NCBI36
NG_052906.1:g.19473_19475del

Transcript Alleles

HGVS Amino-acid Change
ENST00000592092.2:n.248_250del
ENST00000673918.2:c.5876_5878del ENSP00000501283.1:p.Glu1959del
ENST00000674114.2:c.3483_3485del ENSP00000501039.2:n.3483_3485del
ENST00000684977.1:c.1160_1162del ENSP00000509384.1:p.Glu387del
ENST00000689544.1:n.1095_1097del
ENST00000691421.1:c.1163_1165del ENSP00000508674.1:p.Glu388del
ENST00000691855.1:c.5484_5486del
ENST00000692961.1:c.5942_5944del ENSP00000509289.1:p.Glu1981del
ENST00000693677.1:c.704+162_704+164del ENSP00000509779.1:n.704+162_704+164del
ENST00000420124.4:c.5942_5944del MANE Select ENSP00000398837.2:p.Glu1981del
ENST00000673918.1:c.5876_5878del ENSP00000501283.1:p.Glu1959del
ENST00000674114.1:c.3264_3266del
ENST00000420124.2:c.5942_5944del ENSP00000398837.1:p.Glu1981del
NM_014727.2:c.5942_5944del NP_055542.1:p.Glu1981del
XM_011527561.1:c.5876_5878del XP_011525863.1:p.Glu1959del
XM_011527562.1:c.5942_5944del XP_011525864.1:p.Glu1981del
XM_011527563.1:c.5666_5668del XP_011525865.1:p.Glu1889del
XM_011527561.2:c.5378_5380del XP_011525863.2:p.Glu1793del
XM_011527562.2:c.5942_5944del XP_011525864.1:p.Glu1981del
XM_017027544.1:c.5942_5944del XP_016883033.1:p.Glu1981del
XM_017027545.1:c.5378_5380del XP_016883034.1:p.Glu1793del
XM_017027546.1:c.2906_2908del XP_016883035.1:p.Glu969del
NM_014727.3:c.5942_5944del MANE Select NP_055542.1:p.Glu1981del