Canonical Allele Identifier: CA507308702

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36223819T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732918T>G , CM000681.2:g.35732918T>G	GRCh38
NC_000019.9:g.36223819T>G , CM000681.1:g.36223819T>G	GRCh37
NC_000019.8:g.40915659T>G	NCBI36
NG_052906.1:g.19900T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.675T>G
ENST00000673918.2:c.6303T>G	ENSP00000501283.1:p.Gly2101=
ENST00000674114.2:c.3910T>G	ENSP00000501039.2:n.3910T>G
ENST00000684977.1:c.1587T>G	ENSP00000509384.1:p.Gly529=
ENST00000689544.1:n.1522T>G
ENST00000691421.1:c.1590T>G	ENSP00000508674.1:p.Gly530=
ENST00000691855.1:c.5911T>G
ENST00000692961.1:c.6369T>G	ENSP00000509289.1:p.Gly2123=
ENST00000693677.1:c.704+589T>G	ENSP00000509779.1:n.704+589T>G
ENST00000420124.4:c.6369T>G MANE Select	ENSP00000398837.2:p.Gly2123=
ENST00000673918.1:c.6303T>G	ENSP00000501283.1:p.Gly2101=
ENST00000674114.1:c.3691T>G
ENST00000420124.2:c.6369T>G	ENSP00000398837.1:p.Gly2123=
NM_014727.2:c.6369T>G	NP_055542.1:p.Gly2123=
XM_011527561.1:c.6303T>G	XP_011525863.1:p.Gly2101=
XM_011527562.1:c.6369T>G	XP_011525864.1:p.Gly2123=
XM_011527563.1:c.6093T>G	XP_011525865.1:p.Gly2031=
XM_011527561.2:c.5805T>G	XP_011525863.2:p.Gly1935=
XM_011527562.2:c.6369T>G	XP_011525864.1:p.Gly2123=
XM_017027544.1:c.6369T>G	XP_016883033.1:p.Gly2123=
XM_017027545.1:c.5805T>G	XP_016883034.1:p.Gly1935=
XM_017027546.1:c.3333T>G	XP_016883035.1:p.Gly1111=
NM_014727.3:c.6369T>G MANE Select	NP_055542.1:p.Gly2123=