Canonical Allele Identifier: CA507308056

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36223339G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732438G>C , CM000681.2:g.35732438G>C	GRCh38
NC_000019.9:g.36223339G>C , CM000681.1:g.36223339G>C	GRCh37
NC_000019.8:g.40915179G>C	NCBI36
NG_052906.1:g.19420G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.195G>C
ENST00000673918.2:c.5823G>C	ENSP00000501283.1:p.Pro1941=
ENST00000674114.2:c.3430G>C	ENSP00000501039.2:n.3430G>C
ENST00000684977.1:c.1107G>C	ENSP00000509384.1:p.Pro369=
ENST00000689544.1:n.1042G>C
ENST00000691421.1:c.1110G>C	ENSP00000508674.1:p.Pro370=
ENST00000691855.1:c.5431G>C
ENST00000692961.1:c.5889G>C	ENSP00000509289.1:p.Pro1963=
ENST00000693677.1:c.704+109G>C	ENSP00000509779.1:n.704+109G>C
ENST00000420124.4:c.5889G>C MANE Select	ENSP00000398837.2:p.Pro1963=
ENST00000673918.1:c.5823G>C	ENSP00000501283.1:p.Pro1941=
ENST00000674114.1:c.3211G>C
ENST00000420124.2:c.5889G>C	ENSP00000398837.1:p.Pro1963=
NM_014727.2:c.5889G>C	NP_055542.1:p.Pro1963=
XM_011527561.1:c.5823G>C	XP_011525863.1:p.Pro1941=
XM_011527562.1:c.5889G>C	XP_011525864.1:p.Pro1963=
XM_011527563.1:c.5613G>C	XP_011525865.1:p.Pro1871=
XM_011527561.2:c.5325G>C	XP_011525863.2:p.Pro1775=
XM_011527562.2:c.5889G>C	XP_011525864.1:p.Pro1963=
XM_017027544.1:c.5889G>C	XP_016883033.1:p.Pro1963=
XM_017027545.1:c.5325G>C	XP_016883034.1:p.Pro1775=
XM_017027546.1:c.2853G>C	XP_016883035.1:p.Pro951=
NM_014727.3:c.5889G>C MANE Select	NP_055542.1:p.Pro1963=