Canonical Allele Identifier: CA507308291

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36223714A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732813A>G , CM000681.2:g.35732813A>G	GRCh38
NC_000019.9:g.36223714A>G , CM000681.1:g.36223714A>G	GRCh37
NC_000019.8:g.40915554A>G	NCBI36
NG_052906.1:g.19795A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.570A>G
ENST00000673918.2:c.6198A>G	ENSP00000501283.1:p.Pro2066=
ENST00000674114.2:c.3805A>G	ENSP00000501039.2:n.3805A>G
ENST00000684977.1:c.1482A>G	ENSP00000509384.1:p.Pro494=
ENST00000689544.1:n.1417A>G
ENST00000691421.1:c.1485A>G	ENSP00000508674.1:p.Pro495=
ENST00000691855.1:c.5806A>G
ENST00000692961.1:c.6264A>G	ENSP00000509289.1:p.Pro2088=
ENST00000693677.1:c.704+484A>G	ENSP00000509779.1:n.704+484A>G
ENST00000420124.4:c.6264A>G MANE Select	ENSP00000398837.2:p.Pro2088=
ENST00000673918.1:c.6198A>G	ENSP00000501283.1:p.Pro2066=
ENST00000674114.1:c.3586A>G
ENST00000420124.2:c.6264A>G	ENSP00000398837.1:p.Pro2088=
NM_014727.2:c.6264A>G	NP_055542.1:p.Pro2088=
XM_011527561.1:c.6198A>G	XP_011525863.1:p.Pro2066=
XM_011527562.1:c.6264A>G	XP_011525864.1:p.Pro2088=
XM_011527563.1:c.5988A>G	XP_011525865.1:p.Pro1996=
XM_011527561.2:c.5700A>G	XP_011525863.2:p.Pro1900=
XM_011527562.2:c.6264A>G	XP_011525864.1:p.Pro2088=
XM_017027544.1:c.6264A>G	XP_016883033.1:p.Pro2088=
XM_017027545.1:c.5700A>G	XP_016883034.1:p.Pro1900=
XM_017027546.1:c.3228A>G	XP_016883035.1:p.Pro1076=
NM_014727.3:c.6264A>G MANE Select	NP_055542.1:p.Pro2088=