Canonical Allele Identifier: CA2333793096

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35730032C= , CM000681.2:g.35730032C=	GRCh38
NC_000019.9:g.36220933C= , CM000681.1:g.36220933C=	GRCh37
NC_000019.8:g.40912773C=	NCBI36
NG_052906.1:g.17014C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.4917C=	ENSP00000501283.1:p.Asn1639=
ENST00000674114.2:c.2524C=	ENSP00000501039.2:n.2524C=
ENST00000684977.1:c.201C=	ENSP00000509384.1:p.Asn67=
ENST00000685168.1:c.409C=
ENST00000689544.1:n.136C=
ENST00000691421.1:c.204C=	ENSP00000508674.1:p.Asn68=
ENST00000691855.1:c.4525C=
ENST00000692961.1:c.4983C=	ENSP00000509289.1:p.Asn1661=
ENST00000420124.4:c.4983C= MANE Select	ENSP00000398837.2:p.Asn1661=
ENST00000673918.1:c.4917C=	ENSP00000501283.1:p.Asn1639=
ENST00000674114.1:c.2305C=
ENST00000420124.2:c.4983C=	ENSP00000398837.1:p.Asn1661=
NM_014727.2:c.4983C=	NP_055542.1:p.Asn1661=
XM_011527561.1:c.4917C=	XP_011525863.1:p.Asn1639=
XM_011527562.1:c.4983C=	XP_011525864.1:p.Asn1661=
XM_011527563.1:c.4707C=	XP_011525865.1:p.Asn1569=
XM_011527561.2:c.4419C=	XP_011525863.2:p.Asn1473=
XM_011527562.2:c.4983C=	XP_011525864.1:p.Asn1661=
XM_017027544.1:c.4983C=	XP_016883033.1:p.Asn1661=
XM_017027545.1:c.4419C=	XP_016883034.1:p.Asn1473=
XM_017027546.1:c.1947C=	XP_016883035.1:p.Asn649=
NM_014727.3:c.4983C= MANE Select	NP_055542.1:p.Asn1661=