Canonical Allele Identifier: CA2333794587

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732969T= , CM000681.2:g.35732969T=	GRCh38
NC_000019.9:g.36223870T= , CM000681.1:g.36223870T=	GRCh37
NC_000019.8:g.40915710T=	NCBI36
NG_052906.1:g.19951T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.726T=
ENST00000673918.2:c.6354T=	ENSP00000501283.1:p.Pro2118=
ENST00000674114.2:c.3961T=	ENSP00000501039.2:n.3961T=
ENST00000684977.1:c.1638T=	ENSP00000509384.1:p.Pro546=
ENST00000689544.1:n.1573T=
ENST00000691421.1:c.1641T=	ENSP00000508674.1:p.Pro547=
ENST00000691855.1:c.5962T=
ENST00000692961.1:c.6420T=	ENSP00000509289.1:p.Pro2140=
ENST00000693677.1:c.705-628T=	ENSP00000509779.1:n.705-628T=
ENST00000420124.4:c.6420T= MANE Select	ENSP00000398837.2:p.Pro2140=
ENST00000673918.1:c.6354T=	ENSP00000501283.1:p.Pro2118=
ENST00000674114.1:c.3742T=
ENST00000420124.2:c.6420T=	ENSP00000398837.1:p.Pro2140=
NM_014727.2:c.6420T=	NP_055542.1:p.Pro2140=
XM_011527561.1:c.6354T=	XP_011525863.1:p.Pro2118=
XM_011527562.1:c.6420T=	XP_011525864.1:p.Pro2140=
XM_011527563.1:c.6144T=	XP_011525865.1:p.Pro2048=
XM_011527561.2:c.5856T=	XP_011525863.2:p.Pro1952=
XM_011527562.2:c.6420T=	XP_011525864.1:p.Pro2140=
XM_017027544.1:c.6420T=	XP_016883033.1:p.Pro2140=
XM_017027545.1:c.5856T=	XP_016883034.1:p.Pro1952=
XM_017027546.1:c.3384T=	XP_016883035.1:p.Pro1128=
NM_014727.3:c.6420T= MANE Select	NP_055542.1:p.Pro2140=