Canonical Allele Identifier: CA2333794705

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35733206T= , CM000681.2:g.35733206T=	GRCh38
NC_000019.9:g.36224107T= , CM000681.1:g.36224107T=	GRCh37
NC_000019.8:g.40915947T=	NCBI36
NG_052906.1:g.20188T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.963T=
ENST00000673918.2:c.6591T=	ENSP00000501283.1:p.Pro2197=
ENST00000674114.2:c.4198T=	ENSP00000501039.2:n.4198T=
ENST00000684977.1:c.1875T=	ENSP00000509384.1:p.Pro625=
ENST00000689544.1:n.1810T=
ENST00000691421.1:c.1878T=	ENSP00000508674.1:p.Pro626=
ENST00000691855.1:c.6199T=
ENST00000692961.1:c.6657T=	ENSP00000509289.1:p.Pro2219=
ENST00000693677.1:c.705-391T=	ENSP00000509779.1:n.705-391T=
ENST00000420124.4:c.6657T= MANE Select	ENSP00000398837.2:p.Pro2219=
ENST00000673918.1:c.6591T=	ENSP00000501283.1:p.Pro2197=
ENST00000674114.1:c.3979T=
ENST00000420124.2:c.6657T=	ENSP00000398837.1:p.Pro2219=
NM_014727.2:c.6657T=	NP_055542.1:p.Pro2219=
XM_011527561.1:c.6591T=	XP_011525863.1:p.Pro2197=
XM_011527562.1:c.6657T=	XP_011525864.1:p.Pro2219=
XM_011527563.1:c.6381T=	XP_011525865.1:p.Pro2127=
XM_011527561.2:c.6093T=	XP_011525863.2:p.Pro2031=
XM_011527562.2:c.6657T=	XP_011525864.1:p.Pro2219=
XM_017027544.1:c.6657T=	XP_016883033.1:p.Pro2219=
XM_017027545.1:c.6093T=	XP_016883034.1:p.Pro2031=
XM_017027546.1:c.3621T=	XP_016883035.1:p.Pro1207=
NM_014727.3:c.6657T= MANE Select	NP_055542.1:p.Pro2219=