Canonical Allele Identifier: CA507308269

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36223705T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732804T>G , CM000681.2:g.35732804T>G	GRCh38
NC_000019.9:g.36223705T>G , CM000681.1:g.36223705T>G	GRCh37
NC_000019.8:g.40915545T>G	NCBI36
NG_052906.1:g.19786T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.561T>G
ENST00000673918.2:c.6189T>G	ENSP00000501283.1:p.Pro2063=
ENST00000674114.2:c.3796T>G	ENSP00000501039.2:n.3796T>G
ENST00000684977.1:c.1473T>G	ENSP00000509384.1:p.Pro491=
ENST00000689544.1:n.1408T>G
ENST00000691421.1:c.1476T>G	ENSP00000508674.1:p.Pro492=
ENST00000691855.1:c.5797T>G
ENST00000692961.1:c.6255T>G	ENSP00000509289.1:p.Pro2085=
ENST00000693677.1:c.704+475T>G	ENSP00000509779.1:n.704+475T>G
ENST00000420124.4:c.6255T>G MANE Select	ENSP00000398837.2:p.Pro2085=
ENST00000673918.1:c.6189T>G	ENSP00000501283.1:p.Pro2063=
ENST00000674114.1:c.3577T>G
ENST00000420124.2:c.6255T>G	ENSP00000398837.1:p.Pro2085=
NM_014727.2:c.6255T>G	NP_055542.1:p.Pro2085=
XM_011527561.1:c.6189T>G	XP_011525863.1:p.Pro2063=
XM_011527562.1:c.6255T>G	XP_011525864.1:p.Pro2085=
XM_011527563.1:c.5979T>G	XP_011525865.1:p.Pro1993=
XM_011527561.2:c.5691T>G	XP_011525863.2:p.Pro1897=
XM_011527562.2:c.6255T>G	XP_011525864.1:p.Pro2085=
XM_017027544.1:c.6255T>G	XP_016883033.1:p.Pro2085=
XM_017027545.1:c.5691T>G	XP_016883034.1:p.Pro1897=
XM_017027546.1:c.3219T>G	XP_016883035.1:p.Pro1073=
NM_014727.3:c.6255T>G MANE Select	NP_055542.1:p.Pro2085=