Canonical Allele Identifier: CA507308711

Gene: KMT2B

Linked Data

• gnomAD v4: 19-35733155-G-A
• MyVariant Identifiers: chr19:g.36224056G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35733155G>A , CM000681.2:g.35733155G>A	GRCh38
NC_000019.9:g.36224056G>A , CM000681.1:g.36224056G>A	GRCh37
NC_000019.8:g.40915896G>A	NCBI36
NG_052906.1:g.20137G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.912G>A
ENST00000673918.2:c.6540G>A	ENSP00000501283.1:p.Val2180=
ENST00000674114.2:c.4147G>A	ENSP00000501039.2:n.4147G>A
ENST00000684977.1:c.1824G>A	ENSP00000509384.1:p.Val608=
ENST00000689544.1:n.1759G>A
ENST00000691421.1:c.1827G>A	ENSP00000508674.1:p.Val609=
ENST00000691855.1:c.6148G>A
ENST00000692961.1:c.6606G>A	ENSP00000509289.1:p.Val2202=
ENST00000693677.1:c.705-442G>A	ENSP00000509779.1:n.705-442G>A
ENST00000420124.4:c.6606G>A MANE Select	ENSP00000398837.2:p.Val2202=
ENST00000673918.1:c.6540G>A	ENSP00000501283.1:p.Val2180=
ENST00000674114.1:c.3928G>A
ENST00000420124.2:c.6606G>A	ENSP00000398837.1:p.Val2202=
NM_014727.2:c.6606G>A	NP_055542.1:p.Val2202=
XM_011527561.1:c.6540G>A	XP_011525863.1:p.Val2180=
XM_011527562.1:c.6606G>A	XP_011525864.1:p.Val2202=
XM_011527563.1:c.6330G>A	XP_011525865.1:p.Val2110=
XM_011527561.2:c.6042G>A	XP_011525863.2:p.Val2014=
XM_011527562.2:c.6606G>A	XP_011525864.1:p.Val2202=
XM_017027544.1:c.6606G>A	XP_016883033.1:p.Val2202=
XM_017027545.1:c.6042G>A	XP_016883034.1:p.Val2014=
XM_017027546.1:c.3570G>A	XP_016883035.1:p.Val1190=
NM_014727.3:c.6606G>A MANE Select	NP_055542.1:p.Val2202=