Canonical Allele Identifier: CA2333793094

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35730023C= , CM000681.2:g.35730023C=	GRCh38
NC_000019.9:g.36220924C= , CM000681.1:g.36220924C=	GRCh37
NC_000019.8:g.40912764C=	NCBI36
NG_052906.1:g.17005C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.4908C=	ENSP00000501283.1:p.Cys1636=
ENST00000674114.2:c.2515C=	ENSP00000501039.2:n.2515C=
ENST00000684977.1:c.192C=	ENSP00000509384.1:p.Cys64=
ENST00000685168.1:c.400C=
ENST00000689544.1:n.127C=
ENST00000691421.1:c.195C=	ENSP00000508674.1:p.Cys65=
ENST00000691855.1:c.4516C=
ENST00000692961.1:c.4974C=	ENSP00000509289.1:p.Cys1658=
ENST00000420124.4:c.4974C= MANE Select	ENSP00000398837.2:p.Cys1658=
ENST00000673918.1:c.4908C=	ENSP00000501283.1:p.Cys1636=
ENST00000674114.1:c.2296C=
ENST00000420124.2:c.4974C=	ENSP00000398837.1:p.Cys1658=
NM_014727.2:c.4974C=	NP_055542.1:p.Cys1658=
XM_011527561.1:c.4908C=	XP_011525863.1:p.Cys1636=
XM_011527562.1:c.4974C=	XP_011525864.1:p.Cys1658=
XM_011527563.1:c.4698C=	XP_011525865.1:p.Cys1566=
XM_011527561.2:c.4410C=	XP_011525863.2:p.Cys1470=
XM_011527562.2:c.4974C=	XP_011525864.1:p.Cys1658=
XM_017027544.1:c.4974C=	XP_016883033.1:p.Cys1658=
XM_017027545.1:c.4410C=	XP_016883034.1:p.Cys1470=
XM_017027546.1:c.1938C=	XP_016883035.1:p.Cys646=
NM_014727.3:c.4974C= MANE Select	NP_055542.1:p.Cys1658=