Canonical Allele Identifier: CA507308493

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36223765T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732864T>G , CM000681.2:g.35732864T>G	GRCh38
NC_000019.9:g.36223765T>G , CM000681.1:g.36223765T>G	GRCh37
NC_000019.8:g.40915605T>G	NCBI36
NG_052906.1:g.19846T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000592092.2:n.621T>G
ENST00000673918.2:c.6249T>G	ENSP00000501283.1:p.Pro2083=
ENST00000674114.2:c.3856T>G	ENSP00000501039.2:n.3856T>G
ENST00000684977.1:c.1533T>G	ENSP00000509384.1:p.Pro511=
ENST00000689544.1:n.1468T>G
ENST00000691421.1:c.1536T>G	ENSP00000508674.1:p.Pro512=
ENST00000691855.1:c.5857T>G
ENST00000692961.1:c.6315T>G	ENSP00000509289.1:p.Pro2105=
ENST00000693677.1:c.704+535T>G	ENSP00000509779.1:n.704+535T>G
ENST00000420124.4:c.6315T>G MANE Select	ENSP00000398837.2:p.Pro2105=
ENST00000673918.1:c.6249T>G	ENSP00000501283.1:p.Pro2083=
ENST00000674114.1:c.3637T>G
ENST00000420124.2:c.6315T>G	ENSP00000398837.1:p.Pro2105=
NM_014727.2:c.6315T>G	NP_055542.1:p.Pro2105=
XM_011527561.1:c.6249T>G	XP_011525863.1:p.Pro2083=
XM_011527562.1:c.6315T>G	XP_011525864.1:p.Pro2105=
XM_011527563.1:c.6039T>G	XP_011525865.1:p.Pro2013=
XM_011527561.2:c.5751T>G	XP_011525863.2:p.Pro1917=
XM_011527562.2:c.6315T>G	XP_011525864.1:p.Pro2105=
XM_017027544.1:c.6315T>G	XP_016883033.1:p.Pro2105=
XM_017027545.1:c.5751T>G	XP_016883034.1:p.Pro1917=
XM_017027546.1:c.3279T>G	XP_016883035.1:p.Pro1093=
NM_014727.3:c.6315T>G MANE Select	NP_055542.1:p.Pro2105=