Canonical Allele Identifier: CA507308760

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36224664G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35733763G>T , CM000681.2:g.35733763G>T	GRCh38
NC_000019.9:g.36224664G>T , CM000681.1:g.36224664G>T	GRCh37
NC_000019.8:g.40916504G>T	NCBI36
NG_052906.1:g.20745G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000592092.2:n.1520G>T
ENST00000673918.2:c.6984G>T	ENSP00000501283.1:p.Gly2328=
ENST00000674114.2:c.4591G>T	ENSP00000501039.2:n.4591G>T
ENST00000684977.1:c.2245G>T	ENSP00000509384.1:n.2245G>T
ENST00000689544.1:n.2291G>T
ENST00000689929.1:c.1G>T
ENST00000691421.1:c.2181G>T	ENSP00000508674.1:p.Gly727=
ENST00000691855.1:c.6592G>T
ENST00000692961.1:c.6974G>T	ENSP00000509289.1:p.Gly2325Val
ENST00000693175.1:c.1G>T
ENST00000693677.1:c.795G>T	ENSP00000509779.1:p.Gly265=
ENST00000420124.4:c.7050G>T MANE Select	ENSP00000398837.2:p.Gly2350=
ENST00000673918.1:c.6984G>T	ENSP00000501283.1:p.Gly2328=
ENST00000674114.1:c.4372G>T
ENST00000420124.2:c.7050G>T	ENSP00000398837.1:p.Gly2350=
ENST00000592092.1:n.430G>T
NM_014727.2:c.7050G>T	NP_055542.1:p.Gly2350=
XM_011527561.1:c.6984G>T	XP_011525863.1:p.Gly2328=
XM_011527562.1:c.7050G>T	XP_011525864.1:p.Gly2350=
XM_011527563.1:c.6774G>T	XP_011525865.1:p.Gly2258=
XM_011527561.2:c.6486G>T	XP_011525863.2:p.Gly2162=
XM_011527562.2:c.7050G>T	XP_011525864.1:p.Gly2350=
XM_017027544.1:c.6960G>T	XP_016883033.1:p.Gly2320=
XM_017027545.1:c.6486G>T	XP_016883034.1:p.Gly2162=
XM_017027546.1:c.4014G>T	XP_016883035.1:p.Gly1338=
NM_014727.3:c.7050G>T MANE Select	NP_055542.1:p.Gly2350=