Canonical Allele Identifier: CA2584575162

Gene: KMT2B

Linked Data

• gnomAD v4: 19-35732861-GCCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732865_35732867del , CM000681.2:g.35732865_35732867del	GRCh38
NC_000019.9:g.36223766_36223768del , CM000681.1:g.36223766_36223768del	GRCh37
NC_000019.8:g.40915606_40915608del	NCBI36
NG_052906.1:g.19847_19849del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.622_624del
ENST00000673918.2:c.6250_6252del	ENSP00000501283.1:p.Pro2084del
ENST00000674114.2:c.3857_3859del	ENSP00000501039.2:n.3857_3859del
ENST00000684977.1:c.1534_1536del	ENSP00000509384.1:p.Pro512del
ENST00000689544.1:n.1469_1471del
ENST00000691421.1:c.1537_1539del	ENSP00000508674.1:p.Pro513del
ENST00000691855.1:c.5858_5860del
ENST00000692961.1:c.6316_6318del	ENSP00000509289.1:p.Pro2106del
ENST00000693677.1:c.704+536_704+538del	ENSP00000509779.1:n.704+536_704+538del
ENST00000420124.4:c.6316_6318del MANE Select	ENSP00000398837.2:p.Pro2106del
ENST00000673918.1:c.6250_6252del	ENSP00000501283.1:p.Pro2084del
ENST00000674114.1:c.3638_3640del
ENST00000420124.2:c.6316_6318del	ENSP00000398837.1:p.Pro2106del
NM_014727.2:c.6316_6318del	NP_055542.1:p.Pro2106del
XM_011527561.1:c.6250_6252del	XP_011525863.1:p.Pro2084del
XM_011527562.1:c.6316_6318del	XP_011525864.1:p.Pro2106del
XM_011527563.1:c.6040_6042del	XP_011525865.1:p.Pro2014del
XM_011527561.2:c.5752_5754del	XP_011525863.2:p.Pro1918del
XM_011527562.2:c.6316_6318del	XP_011525864.1:p.Pro2106del
XM_017027544.1:c.6316_6318del	XP_016883033.1:p.Pro2106del
XM_017027545.1:c.5752_5754del	XP_016883034.1:p.Pro1918del
XM_017027546.1:c.3280_3282del	XP_016883035.1:p.Pro1094del
NM_014727.3:c.6316_6318del MANE Select	NP_055542.1:p.Pro2106del