Canonical Allele Identifier: CA405427884

Gene: KMT2B

Linked Data

• dbSNP Id: rs369549803
• MyVariant Identifiers: chr19:g.36223789T>G (hg19) ; chr19:g.35732888T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732888T>G , CM000681.2:g.35732888T>G	GRCh38
NC_000019.9:g.36223789T>G , CM000681.1:g.36223789T>G	GRCh37
NC_000019.8:g.40915629T>G	NCBI36
NG_052906.1:g.19870T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.645T>G
ENST00000673918.2:c.6273T>G	ENSP00000501283.1:p.Ile2091Met
ENST00000674114.2:c.3880T>G	ENSP00000501039.2:n.3880T>G
ENST00000684977.1:c.1557T>G	ENSP00000509384.1:p.Ile519Met
ENST00000689544.1:n.1492T>G
ENST00000691421.1:c.1560T>G	ENSP00000508674.1:p.Ile520Met
ENST00000691855.1:c.5881T>G
ENST00000692961.1:c.6339T>G	ENSP00000509289.1:p.Ile2113Met
ENST00000693677.1:c.704+559T>G	ENSP00000509779.1:n.704+559T>G
ENST00000420124.4:c.6339T>G MANE Select	ENSP00000398837.2:p.Ile2113Met
ENST00000673918.1:c.6273T>G	ENSP00000501283.1:p.Ile2091Met
ENST00000674114.1:c.3661T>G
ENST00000420124.2:c.6339T>G	ENSP00000398837.1:p.Ile2113Met
NM_014727.2:c.6339T>G	NP_055542.1:p.Ile2113Met
XM_011527561.1:c.6273T>G	XP_011525863.1:p.Ile2091Met
XM_011527562.1:c.6339T>G	XP_011525864.1:p.Ile2113Met
XM_011527563.1:c.6063T>G	XP_011525865.1:p.Ile2021Met
XM_011527561.2:c.5775T>G	XP_011525863.2:p.Ile1925Met
XM_011527562.2:c.6339T>G	XP_011525864.1:p.Ile2113Met
XM_017027544.1:c.6339T>G	XP_016883033.1:p.Ile2113Met
XM_017027545.1:c.5775T>G	XP_016883034.1:p.Ile1925Met
XM_017027546.1:c.3303T>G	XP_016883035.1:p.Ile1101Met
NM_014727.3:c.6339T>G MANE Select	NP_055542.1:p.Ile2113Met