Canonical Allele Identifier: CA507308275

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36223492G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732591G>C , CM000681.2:g.35732591G>C	GRCh38
NC_000019.9:g.36223492G>C , CM000681.1:g.36223492G>C	GRCh37
NC_000019.8:g.40915332G>C	NCBI36
NG_052906.1:g.19573G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.348G>C
ENST00000673918.2:c.5976G>C	ENSP00000501283.1:p.Gly1992=
ENST00000674114.2:c.3583G>C	ENSP00000501039.2:n.3583G>C
ENST00000684977.1:c.1260G>C	ENSP00000509384.1:p.Gly420=
ENST00000689544.1:n.1195G>C
ENST00000691421.1:c.1263G>C	ENSP00000508674.1:p.Gly421=
ENST00000691855.1:c.5584G>C
ENST00000692961.1:c.6042G>C	ENSP00000509289.1:p.Gly2014=
ENST00000693677.1:c.704+262G>C	ENSP00000509779.1:n.704+262G>C
ENST00000420124.4:c.6042G>C MANE Select	ENSP00000398837.2:p.Gly2014=
ENST00000673918.1:c.5976G>C	ENSP00000501283.1:p.Gly1992=
ENST00000674114.1:c.3364G>C
ENST00000420124.2:c.6042G>C	ENSP00000398837.1:p.Gly2014=
NM_014727.2:c.6042G>C	NP_055542.1:p.Gly2014=
XM_011527561.1:c.5976G>C	XP_011525863.1:p.Gly1992=
XM_011527562.1:c.6042G>C	XP_011525864.1:p.Gly2014=
XM_011527563.1:c.5766G>C	XP_011525865.1:p.Gly1922=
XM_011527561.2:c.5478G>C	XP_011525863.2:p.Gly1826=
XM_011527562.2:c.6042G>C	XP_011525864.1:p.Gly2014=
XM_017027544.1:c.6042G>C	XP_016883033.1:p.Gly2014=
XM_017027545.1:c.5478G>C	XP_016883034.1:p.Gly1826=
XM_017027546.1:c.3006G>C	XP_016883035.1:p.Gly1002=
NM_014727.3:c.6042G>C MANE Select	NP_055542.1:p.Gly2014=