Canonical Allele Identifier: CA507309129

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36223936A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35733035A>C , CM000681.2:g.35733035A>C	GRCh38
NC_000019.9:g.36223936A>C , CM000681.1:g.36223936A>C	GRCh37
NC_000019.8:g.40915776A>C	NCBI36
NG_052906.1:g.20017A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.792A>C
ENST00000673918.2:c.6420A>C	ENSP00000501283.1:p.Thr2140=
ENST00000674114.2:c.4027A>C	ENSP00000501039.2:n.4027A>C
ENST00000684977.1:c.1704A>C	ENSP00000509384.1:p.Thr568=
ENST00000689544.1:n.1639A>C
ENST00000691421.1:c.1707A>C	ENSP00000508674.1:p.Thr569=
ENST00000691855.1:c.6028A>C
ENST00000692961.1:c.6486A>C	ENSP00000509289.1:p.Thr2162=
ENST00000693677.1:c.705-562A>C	ENSP00000509779.1:n.705-562A>C
ENST00000420124.4:c.6486A>C MANE Select	ENSP00000398837.2:p.Thr2162=
ENST00000673918.1:c.6420A>C	ENSP00000501283.1:p.Thr2140=
ENST00000674114.1:c.3808A>C
ENST00000420124.2:c.6486A>C	ENSP00000398837.1:p.Thr2162=
NM_014727.2:c.6486A>C	NP_055542.1:p.Thr2162=
XM_011527561.1:c.6420A>C	XP_011525863.1:p.Thr2140=
XM_011527562.1:c.6486A>C	XP_011525864.1:p.Thr2162=
XM_011527563.1:c.6210A>C	XP_011525865.1:p.Thr2070=
XM_011527561.2:c.5922A>C	XP_011525863.2:p.Thr1974=
XM_011527562.2:c.6486A>C	XP_011525864.1:p.Thr2162=
XM_017027544.1:c.6486A>C	XP_016883033.1:p.Thr2162=
XM_017027545.1:c.5922A>C	XP_016883034.1:p.Thr1974=
XM_017027546.1:c.3450A>C	XP_016883035.1:p.Thr1150=
NM_014727.3:c.6486A>C MANE Select	NP_055542.1:p.Thr2162=