Canonical Allele Identifier: CA2584575174

Gene: KMT2B

Linked Data

• gnomAD v4: 19-35733213-CCCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35733217_35733219del , CM000681.2:g.35733217_35733219del	GRCh38
NC_000019.9:g.36224118_36224120del , CM000681.1:g.36224118_36224120del	GRCh37
NC_000019.8:g.40915958_40915960del	NCBI36
NG_052906.1:g.20199_20201del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.974_976del
ENST00000673918.2:c.6602_6604del	ENSP00000501283.1:p.Thr2201del
ENST00000674114.2:c.4209_4211del	ENSP00000501039.2:n.4209_4211del
ENST00000684977.1:c.1886_1888del	ENSP00000509384.1:p.Thr629del
ENST00000689544.1:n.1821_1823del
ENST00000691421.1:c.1889_1891del	ENSP00000508674.1:p.Thr630del
ENST00000691855.1:c.6210_6212del
ENST00000692961.1:c.6668_6670del	ENSP00000509289.1:p.Thr2223del
ENST00000693677.1:c.705-380_705-378del	ENSP00000509779.1:n.705-380_705-378del
ENST00000420124.4:c.6668_6670del MANE Select	ENSP00000398837.2:p.Thr2223del
ENST00000673918.1:c.6602_6604del	ENSP00000501283.1:p.Thr2201del
ENST00000674114.1:c.3990_3992del
ENST00000420124.2:c.6668_6670del	ENSP00000398837.1:p.Thr2223del
NM_014727.2:c.6668_6670del	NP_055542.1:p.Thr2223del
XM_011527561.1:c.6602_6604del	XP_011525863.1:p.Thr2201del
XM_011527562.1:c.6668_6670del	XP_011525864.1:p.Thr2223del
XM_011527563.1:c.6392_6394del	XP_011525865.1:p.Thr2131del
XM_011527561.2:c.6104_6106del	XP_011525863.2:p.Thr2035del
XM_011527562.2:c.6668_6670del	XP_011525864.1:p.Thr2223del
XM_017027544.1:c.6668_6670del	XP_016883033.1:p.Thr2223del
XM_017027545.1:c.6104_6106del	XP_016883034.1:p.Thr2035del
XM_017027546.1:c.3632_3634del	XP_016883035.1:p.Thr1211del
NM_014727.3:c.6668_6670del MANE Select	NP_055542.1:p.Thr2223del