Canonical Allele Identifier: CA405428702

Gene: KMT2B

Linked Data

• gnomAD v4: 19-35733019-C-A
• MyVariant Identifiers: chr19:g.36223920C>A (hg19) ; chr19:g.35733019C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35733019C>A , CM000681.2:g.35733019C>A	GRCh38
NC_000019.9:g.36223920C>A , CM000681.1:g.36223920C>A	GRCh37
NC_000019.8:g.40915760C>A	NCBI36
NG_052906.1:g.20001C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.776C>A
ENST00000673918.2:c.6404C>A	ENSP00000501283.1:p.Ala2135Asp
ENST00000674114.2:c.4011C>A	ENSP00000501039.2:n.4011C>A
ENST00000684977.1:c.1688C>A	ENSP00000509384.1:p.Ala563Asp
ENST00000689544.1:n.1623C>A
ENST00000691421.1:c.1691C>A	ENSP00000508674.1:p.Ala564Asp
ENST00000691855.1:c.6012C>A
ENST00000692961.1:c.6470C>A	ENSP00000509289.1:p.Ala2157Asp
ENST00000693677.1:c.705-578C>A	ENSP00000509779.1:n.705-578C>A
ENST00000420124.4:c.6470C>A MANE Select	ENSP00000398837.2:p.Ala2157Asp
ENST00000673918.1:c.6404C>A	ENSP00000501283.1:p.Ala2135Asp
ENST00000674114.1:c.3792C>A
ENST00000420124.2:c.6470C>A	ENSP00000398837.1:p.Ala2157Asp
NM_014727.2:c.6470C>A	NP_055542.1:p.Ala2157Asp
XM_011527561.1:c.6404C>A	XP_011525863.1:p.Ala2135Asp
XM_011527562.1:c.6470C>A	XP_011525864.1:p.Ala2157Asp
XM_011527563.1:c.6194C>A	XP_011525865.1:p.Ala2065Asp
XM_011527561.2:c.5906C>A	XP_011525863.2:p.Ala1969Asp
XM_011527562.2:c.6470C>A	XP_011525864.1:p.Ala2157Asp
XM_017027544.1:c.6470C>A	XP_016883033.1:p.Ala2157Asp
XM_017027545.1:c.5906C>A	XP_016883034.1:p.Ala1969Asp
XM_017027546.1:c.3434C>A	XP_016883035.1:p.Ala1145Asp
NM_014727.3:c.6470C>A MANE Select	NP_055542.1:p.Ala2157Asp