Canonical Allele Identifier: CA9385674

Gene: KMT2B

Linked Data

• dbSNP Id: rs750980005
• ExAC: 19:36223831 A / G
• gnomAD v4: 19-35732930-A-G
• MyVariant Identifiers: chr19:g.36223831A>G (hg19) ; chr19:g.35732930A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732930A>G , CM000681.2:g.35732930A>G	GRCh38
NC_000019.9:g.36223831A>G , CM000681.1:g.36223831A>G	GRCh37
NC_000019.8:g.40915671A>G	NCBI36
NG_052906.1:g.19912A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.687A>G
ENST00000673918.2:c.6315A>G	ENSP00000501283.1:p.Gly2105=
ENST00000674114.2:c.3922A>G	ENSP00000501039.2:n.3922A>G
ENST00000684977.1:c.1599A>G	ENSP00000509384.1:p.Gly533=
ENST00000689544.1:n.1534A>G
ENST00000691421.1:c.1602A>G	ENSP00000508674.1:p.Gly534=
ENST00000691855.1:c.5923A>G
ENST00000692961.1:c.6381A>G	ENSP00000509289.1:p.Gly2127=
ENST00000693677.1:c.704+601A>G	ENSP00000509779.1:n.704+601A>G
ENST00000420124.4:c.6381A>G MANE Select	ENSP00000398837.2:p.Gly2127=
ENST00000673918.1:c.6315A>G	ENSP00000501283.1:p.Gly2105=
ENST00000674114.1:c.3703A>G
ENST00000420124.2:c.6381A>G	ENSP00000398837.1:p.Gly2127=
NM_014727.2:c.6381A>G	NP_055542.1:p.Gly2127=
XM_011527561.1:c.6315A>G	XP_011525863.1:p.Gly2105=
XM_011527562.1:c.6381A>G	XP_011525864.1:p.Gly2127=
XM_011527563.1:c.6105A>G	XP_011525865.1:p.Gly2035=
XM_011527561.2:c.5817A>G	XP_011525863.2:p.Gly1939=
XM_011527562.2:c.6381A>G	XP_011525864.1:p.Gly2127=
XM_017027544.1:c.6381A>G	XP_016883033.1:p.Gly2127=
XM_017027545.1:c.5817A>G	XP_016883034.1:p.Gly1939=
XM_017027546.1:c.3345A>G	XP_016883035.1:p.Gly1115=
NM_014727.3:c.6381A>G MANE Select	NP_055542.1:p.Gly2127=