Canonical Allele Identifier: CA2333793084

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35729999G= , CM000681.2:g.35729999G=	GRCh38
NC_000019.9:g.36220900G= , CM000681.1:g.36220900G=	GRCh37
NC_000019.8:g.40912740G=	NCBI36
NG_052906.1:g.16981G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.4884G=	ENSP00000501283.1:p.Thr1628=
ENST00000674114.2:c.2491G=	ENSP00000501039.2:n.2491G=
ENST00000684977.1:c.168G=	ENSP00000509384.1:p.Thr56=
ENST00000685168.1:c.376G=
ENST00000689544.1:n.103G=
ENST00000691421.1:c.171G=	ENSP00000508674.1:p.Thr57=
ENST00000691855.1:c.4492G=
ENST00000692961.1:c.4950G=	ENSP00000509289.1:p.Thr1650=
ENST00000420124.4:c.4950G= MANE Select	ENSP00000398837.2:p.Thr1650=
ENST00000673918.1:c.4884G=	ENSP00000501283.1:p.Thr1628=
ENST00000674114.1:c.2272G=
ENST00000420124.2:c.4950G=	ENSP00000398837.1:p.Thr1650=
NM_014727.2:c.4950G=	NP_055542.1:p.Thr1650=
XM_011527561.1:c.4884G=	XP_011525863.1:p.Thr1628=
XM_011527562.1:c.4950G=	XP_011525864.1:p.Thr1650=
XM_011527563.1:c.4674G=	XP_011525865.1:p.Thr1558=
XM_011527561.2:c.4386G=	XP_011525863.2:p.Thr1462=
XM_011527562.2:c.4950G=	XP_011525864.1:p.Thr1650=
XM_017027544.1:c.4950G=	XP_016883033.1:p.Thr1650=
XM_017027545.1:c.4386G=	XP_016883034.1:p.Thr1462=
XM_017027546.1:c.1914G=	XP_016883035.1:p.Thr638=
NM_014727.3:c.4950G= MANE Select	NP_055542.1:p.Thr1650=