Canonical Allele Identifier: CA507308861

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36223864G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732963G>C , CM000681.2:g.35732963G>C	GRCh38
NC_000019.9:g.36223864G>C , CM000681.1:g.36223864G>C	GRCh37
NC_000019.8:g.40915704G>C	NCBI36
NG_052906.1:g.19945G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000592092.2:n.720G>C
ENST00000673918.2:c.6348G>C	ENSP00000501283.1:p.Pro2116=
ENST00000674114.2:c.3955G>C	ENSP00000501039.2:n.3955G>C
ENST00000684977.1:c.1632G>C	ENSP00000509384.1:p.Pro544=
ENST00000689544.1:n.1567G>C
ENST00000691421.1:c.1635G>C	ENSP00000508674.1:p.Pro545=
ENST00000691855.1:c.5956G>C
ENST00000692961.1:c.6414G>C	ENSP00000509289.1:p.Pro2138=
ENST00000693677.1:c.705-634G>C	ENSP00000509779.1:n.705-634G>C
ENST00000420124.4:c.6414G>C MANE Select	ENSP00000398837.2:p.Pro2138=
ENST00000673918.1:c.6348G>C	ENSP00000501283.1:p.Pro2116=
ENST00000674114.1:c.3736G>C
ENST00000420124.2:c.6414G>C	ENSP00000398837.1:p.Pro2138=
NM_014727.2:c.6414G>C	NP_055542.1:p.Pro2138=
XM_011527561.1:c.6348G>C	XP_011525863.1:p.Pro2116=
XM_011527562.1:c.6414G>C	XP_011525864.1:p.Pro2138=
XM_011527563.1:c.6138G>C	XP_011525865.1:p.Pro2046=
XM_011527561.2:c.5850G>C	XP_011525863.2:p.Pro1950=
XM_011527562.2:c.6414G>C	XP_011525864.1:p.Pro2138=
XM_017027544.1:c.6414G>C	XP_016883033.1:p.Pro2138=
XM_017027545.1:c.5850G>C	XP_016883034.1:p.Pro1950=
XM_017027546.1:c.3378G>C	XP_016883035.1:p.Pro1126=
NM_014727.3:c.6414G>C MANE Select	NP_055542.1:p.Pro2138=