Canonical Allele Identifier: CA507308256

Gene: KMT2B

Linked Data

• gnomAD v4: 19-35732801-T-G
• MyVariant Identifiers: chr19:g.36223702T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732801T>G , CM000681.2:g.35732801T>G	GRCh38
NC_000019.9:g.36223702T>G , CM000681.1:g.36223702T>G	GRCh37
NC_000019.8:g.40915542T>G	NCBI36
NG_052906.1:g.19783T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.558T>G
ENST00000673918.2:c.6186T>G	ENSP00000501283.1:p.Pro2062=
ENST00000674114.2:c.3793T>G	ENSP00000501039.2:n.3793T>G
ENST00000684977.1:c.1470T>G	ENSP00000509384.1:p.Pro490=
ENST00000689544.1:n.1405T>G
ENST00000691421.1:c.1473T>G	ENSP00000508674.1:p.Pro491=
ENST00000691855.1:c.5794T>G
ENST00000692961.1:c.6252T>G	ENSP00000509289.1:p.Pro2084=
ENST00000693677.1:c.704+472T>G	ENSP00000509779.1:n.704+472T>G
ENST00000420124.4:c.6252T>G MANE Select	ENSP00000398837.2:p.Pro2084=
ENST00000673918.1:c.6186T>G	ENSP00000501283.1:p.Pro2062=
ENST00000674114.1:c.3574T>G
ENST00000420124.2:c.6252T>G	ENSP00000398837.1:p.Pro2084=
NM_014727.2:c.6252T>G	NP_055542.1:p.Pro2084=
XM_011527561.1:c.6186T>G	XP_011525863.1:p.Pro2062=
XM_011527562.1:c.6252T>G	XP_011525864.1:p.Pro2084=
XM_011527563.1:c.5976T>G	XP_011525865.1:p.Pro1992=
XM_011527561.2:c.5688T>G	XP_011525863.2:p.Pro1896=
XM_011527562.2:c.6252T>G	XP_011525864.1:p.Pro2084=
XM_017027544.1:c.6252T>G	XP_016883033.1:p.Pro2084=
XM_017027545.1:c.5688T>G	XP_016883034.1:p.Pro1896=
XM_017027546.1:c.3216T>G	XP_016883035.1:p.Pro1072=
NM_014727.3:c.6252T>G MANE Select	NP_055542.1:p.Pro2084=