Canonical Allele Identifier: CA507308405

Gene: KMT2B

Linked Data

• gnomAD v4: 19-35733077-C-T
• MyVariant Identifiers: chr19:g.36223978C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35733077C>T , CM000681.2:g.35733077C>T	GRCh38
NC_000019.9:g.36223978C>T , CM000681.1:g.36223978C>T	GRCh37
NC_000019.8:g.40915818C>T	NCBI36
NG_052906.1:g.20059C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.834C>T
ENST00000673918.2:c.6462C>T	ENSP00000501283.1:p.Ser2154=
ENST00000674114.2:c.4069C>T	ENSP00000501039.2:n.4069C>T
ENST00000684977.1:c.1746C>T	ENSP00000509384.1:p.Ser582=
ENST00000689544.1:n.1681C>T
ENST00000691421.1:c.1749C>T	ENSP00000508674.1:p.Ser583=
ENST00000691855.1:c.6070C>T
ENST00000692961.1:c.6528C>T	ENSP00000509289.1:p.Ser2176=
ENST00000693677.1:c.705-520C>T	ENSP00000509779.1:n.705-520C>T
ENST00000420124.4:c.6528C>T MANE Select	ENSP00000398837.2:p.Ser2176=
ENST00000673918.1:c.6462C>T	ENSP00000501283.1:p.Ser2154=
ENST00000674114.1:c.3850C>T
ENST00000420124.2:c.6528C>T	ENSP00000398837.1:p.Ser2176=
NM_014727.2:c.6528C>T	NP_055542.1:p.Ser2176=
XM_011527561.1:c.6462C>T	XP_011525863.1:p.Ser2154=
XM_011527562.1:c.6528C>T	XP_011525864.1:p.Ser2176=
XM_011527563.1:c.6252C>T	XP_011525865.1:p.Ser2084=
XM_011527561.2:c.5964C>T	XP_011525863.2:p.Ser1988=
XM_011527562.2:c.6528C>T	XP_011525864.1:p.Ser2176=
XM_017027544.1:c.6528C>T	XP_016883033.1:p.Ser2176=
XM_017027545.1:c.5964C>T	XP_016883034.1:p.Ser1988=
XM_017027546.1:c.3492C>T	XP_016883035.1:p.Ser1164=
NM_014727.3:c.6528C>T MANE Select	NP_055542.1:p.Ser2176=