Canonical Allele Identifier: CA2333794513

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732806C= , CM000681.2:g.35732806C=	GRCh38
NC_000019.9:g.36223707C= , CM000681.1:g.36223707C=	GRCh37
NC_000019.8:g.40915547C=	NCBI36
NG_052906.1:g.19788C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.563C=
ENST00000673918.2:c.6191C=	ENSP00000501283.1:p.Ser2064=
ENST00000674114.2:c.3798C=	ENSP00000501039.2:n.3798C=
ENST00000684977.1:c.1475C=	ENSP00000509384.1:p.Ser492=
ENST00000689544.1:n.1410C=
ENST00000691421.1:c.1478C=	ENSP00000508674.1:p.Ser493=
ENST00000691855.1:c.5799C=
ENST00000692961.1:c.6257C=	ENSP00000509289.1:p.Ser2086=
ENST00000693677.1:c.704+477C=	ENSP00000509779.1:n.704+477C=
ENST00000420124.4:c.6257C= MANE Select	ENSP00000398837.2:p.Ser2086=
ENST00000673918.1:c.6191C=	ENSP00000501283.1:p.Ser2064=
ENST00000674114.1:c.3579C=
ENST00000420124.2:c.6257C=	ENSP00000398837.1:p.Ser2086=
NM_014727.2:c.6257C=	NP_055542.1:p.Ser2086=
XM_011527561.1:c.6191C=	XP_011525863.1:p.Ser2064=
XM_011527562.1:c.6257C=	XP_011525864.1:p.Ser2086=
XM_011527563.1:c.5981C=	XP_011525865.1:p.Ser1994=
XM_011527561.2:c.5693C=	XP_011525863.2:p.Ser1898=
XM_011527562.2:c.6257C=	XP_011525864.1:p.Ser2086=
XM_017027544.1:c.6257C=	XP_016883033.1:p.Ser2086=
XM_017027545.1:c.5693C=	XP_016883034.1:p.Ser1898=
XM_017027546.1:c.3221C=	XP_016883035.1:p.Ser1074=
NM_014727.3:c.6257C= MANE Select	NP_055542.1:p.Ser2086=