Canonical Allele Identifier: CA2333794577

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732956T= , CM000681.2:g.35732956T=	GRCh38
NC_000019.9:g.36223857T= , CM000681.1:g.36223857T=	GRCh37
NC_000019.8:g.40915697T=	NCBI36
NG_052906.1:g.19938T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000592092.2:n.713T=
ENST00000673918.2:c.6341T=	ENSP00000501283.1:p.Leu2114=
ENST00000674114.2:c.3948T=	ENSP00000501039.2:n.3948T=
ENST00000684977.1:c.1625T=	ENSP00000509384.1:p.Leu542=
ENST00000689544.1:n.1560T=
ENST00000691421.1:c.1628T=	ENSP00000508674.1:p.Leu543=
ENST00000691855.1:c.5949T=
ENST00000692961.1:c.6407T=	ENSP00000509289.1:p.Leu2136=
ENST00000693677.1:c.704+627T=	ENSP00000509779.1:n.704+627T=
ENST00000420124.4:c.6407T= MANE Select	ENSP00000398837.2:p.Leu2136=
ENST00000673918.1:c.6341T=	ENSP00000501283.1:p.Leu2114=
ENST00000674114.1:c.3729T=
ENST00000420124.2:c.6407T=	ENSP00000398837.1:p.Leu2136=
NM_014727.2:c.6407T=	NP_055542.1:p.Leu2136=
XM_011527561.1:c.6341T=	XP_011525863.1:p.Leu2114=
XM_011527562.1:c.6407T=	XP_011525864.1:p.Leu2136=
XM_011527563.1:c.6131T=	XP_011525865.1:p.Leu2044=
XM_011527561.2:c.5843T=	XP_011525863.2:p.Leu1948=
XM_011527562.2:c.6407T=	XP_011525864.1:p.Leu2136=
XM_017027544.1:c.6407T=	XP_016883033.1:p.Leu2136=
XM_017027545.1:c.5843T=	XP_016883034.1:p.Leu1948=
XM_017027546.1:c.3371T=	XP_016883035.1:p.Leu1124=
NM_014727.3:c.6407T= MANE Select	NP_055542.1:p.Leu2136=