Canonical Allele Identifier: CA507072632

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36220951C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35730050C>A , CM000681.2:g.35730050C>A	GRCh38
NC_000019.9:g.36220951C>A , CM000681.1:g.36220951C>A	GRCh37
NC_000019.8:g.40912791C>A	NCBI36
NG_052906.1:g.17032C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.4935C>A	ENSP00000501283.1:p.Ala1645=
ENST00000674114.2:c.2542C>A	ENSP00000501039.2:n.2542C>A
ENST00000684977.1:c.219C>A	ENSP00000509384.1:p.Ala73=
ENST00000685168.1:c.427C>A
ENST00000689544.1:n.154C>A
ENST00000691421.1:c.222C>A	ENSP00000508674.1:p.Ala74=
ENST00000691855.1:c.4543C>A
ENST00000692961.1:c.5001C>A	ENSP00000509289.1:p.Ala1667=
ENST00000420124.4:c.5001C>A MANE Select	ENSP00000398837.2:p.Ala1667=
ENST00000673918.1:c.4935C>A	ENSP00000501283.1:p.Ala1645=
ENST00000674114.1:c.2323C>A
ENST00000420124.2:c.5001C>A	ENSP00000398837.1:p.Ala1667=
NM_014727.2:c.5001C>A	NP_055542.1:p.Ala1667=
XM_011527561.1:c.4935C>A	XP_011525863.1:p.Ala1645=
XM_011527562.1:c.5001C>A	XP_011525864.1:p.Ala1667=
XM_011527563.1:c.4725C>A	XP_011525865.1:p.Ala1575=
XM_011527561.2:c.4437C>A	XP_011525863.2:p.Ala1479=
XM_011527562.2:c.5001C>A	XP_011525864.1:p.Ala1667=
XM_017027544.1:c.5001C>A	XP_016883033.1:p.Ala1667=
XM_017027545.1:c.4437C>A	XP_016883034.1:p.Ala1479=
XM_017027546.1:c.1965C>A	XP_016883035.1:p.Ala655=
NM_014727.3:c.5001C>A MANE Select	NP_055542.1:p.Ala1667=