Canonical Allele Identifier: CA507308552

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36223591G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732690G>C , CM000681.2:g.35732690G>C	GRCh38
NC_000019.9:g.36223591G>C , CM000681.1:g.36223591G>C	GRCh37
NC_000019.8:g.40915431G>C	NCBI36
NG_052906.1:g.19672G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.447G>C
ENST00000673918.2:c.6075G>C	ENSP00000501283.1:p.Leu2025=
ENST00000674114.2:c.3682G>C	ENSP00000501039.2:n.3682G>C
ENST00000684977.1:c.1359G>C	ENSP00000509384.1:p.Leu453=
ENST00000689544.1:n.1294G>C
ENST00000691421.1:c.1362G>C	ENSP00000508674.1:p.Leu454=
ENST00000691855.1:c.5683G>C
ENST00000692961.1:c.6141G>C	ENSP00000509289.1:p.Leu2047=
ENST00000693677.1:c.704+361G>C	ENSP00000509779.1:n.704+361G>C
ENST00000420124.4:c.6141G>C MANE Select	ENSP00000398837.2:p.Leu2047=
ENST00000673918.1:c.6075G>C	ENSP00000501283.1:p.Leu2025=
ENST00000674114.1:c.3463G>C
ENST00000420124.2:c.6141G>C	ENSP00000398837.1:p.Leu2047=
NM_014727.2:c.6141G>C	NP_055542.1:p.Leu2047=
XM_011527561.1:c.6075G>C	XP_011525863.1:p.Leu2025=
XM_011527562.1:c.6141G>C	XP_011525864.1:p.Leu2047=
XM_011527563.1:c.5865G>C	XP_011525865.1:p.Leu1955=
XM_011527561.2:c.5577G>C	XP_011525863.2:p.Leu1859=
XM_011527562.2:c.6141G>C	XP_011525864.1:p.Leu2047=
XM_017027544.1:c.6141G>C	XP_016883033.1:p.Leu2047=
XM_017027545.1:c.5577G>C	XP_016883034.1:p.Leu1859=
XM_017027546.1:c.3105G>C	XP_016883035.1:p.Leu1035=
NM_014727.3:c.6141G>C MANE Select	NP_055542.1:p.Leu2047=