Canonical Allele Identifier: CA507072687

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36220990C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35730089C>A , CM000681.2:g.35730089C>A	GRCh38
NC_000019.9:g.36220990C>A , CM000681.1:g.36220990C>A	GRCh37
NC_000019.8:g.40912830C>A	NCBI36
NG_052906.1:g.17071C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.4974C>A	ENSP00000501283.1:p.Val1658=
ENST00000674114.2:c.2581C>A	ENSP00000501039.2:n.2581C>A
ENST00000684977.1:c.258C>A	ENSP00000509384.1:p.Val86=
ENST00000685168.1:c.466C>A
ENST00000689544.1:n.193C>A
ENST00000691421.1:c.261C>A	ENSP00000508674.1:p.Val87=
ENST00000691855.1:c.4582C>A
ENST00000692961.1:c.5040C>A	ENSP00000509289.1:p.Val1680=
ENST00000420124.4:c.5040C>A MANE Select	ENSP00000398837.2:p.Val1680=
ENST00000673918.1:c.4974C>A	ENSP00000501283.1:p.Val1658=
ENST00000674114.1:c.2362C>A
ENST00000420124.2:c.5040C>A	ENSP00000398837.1:p.Val1680=
NM_014727.2:c.5040C>A	NP_055542.1:p.Val1680=
XM_011527561.1:c.4974C>A	XP_011525863.1:p.Val1658=
XM_011527562.1:c.5040C>A	XP_011525864.1:p.Val1680=
XM_011527563.1:c.4764C>A	XP_011525865.1:p.Val1588=
XM_011527561.2:c.4476C>A	XP_011525863.2:p.Val1492=
XM_011527562.2:c.5040C>A	XP_011525864.1:p.Val1680=
XM_017027544.1:c.5040C>A	XP_016883033.1:p.Val1680=
XM_017027545.1:c.4476C>A	XP_016883034.1:p.Val1492=
XM_017027546.1:c.2004C>A	XP_016883035.1:p.Val668=
NM_014727.3:c.5040C>A MANE Select	NP_055542.1:p.Val1680=