Canonical Allele Identifier: CA507308692

Gene: KMT2B

Linked Data

• gnomAD v4: 19-35732915-G-T
• MyVariant Identifiers: chr19:g.36223816G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732915G>T , CM000681.2:g.35732915G>T	GRCh38
NC_000019.9:g.36223816G>T , CM000681.1:g.36223816G>T	GRCh37
NC_000019.8:g.40915656G>T	NCBI36
NG_052906.1:g.19897G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.672G>T
ENST00000673918.2:c.6300G>T	ENSP00000501283.1:p.Gly2100=
ENST00000674114.2:c.3907G>T	ENSP00000501039.2:n.3907G>T
ENST00000684977.1:c.1584G>T	ENSP00000509384.1:p.Gly528=
ENST00000689544.1:n.1519G>T
ENST00000691421.1:c.1587G>T	ENSP00000508674.1:p.Gly529=
ENST00000691855.1:c.5908G>T
ENST00000692961.1:c.6366G>T	ENSP00000509289.1:p.Gly2122=
ENST00000693677.1:c.704+586G>T	ENSP00000509779.1:n.704+586G>T
ENST00000420124.4:c.6366G>T MANE Select	ENSP00000398837.2:p.Gly2122=
ENST00000673918.1:c.6300G>T	ENSP00000501283.1:p.Gly2100=
ENST00000674114.1:c.3688G>T
ENST00000420124.2:c.6366G>T	ENSP00000398837.1:p.Gly2122=
NM_014727.2:c.6366G>T	NP_055542.1:p.Gly2122=
XM_011527561.1:c.6300G>T	XP_011525863.1:p.Gly2100=
XM_011527562.1:c.6366G>T	XP_011525864.1:p.Gly2122=
XM_011527563.1:c.6090G>T	XP_011525865.1:p.Gly2030=
XM_011527561.2:c.5802G>T	XP_011525863.2:p.Gly1934=
XM_011527562.2:c.6366G>T	XP_011525864.1:p.Gly2122=
XM_017027544.1:c.6366G>T	XP_016883033.1:p.Gly2122=
XM_017027545.1:c.5802G>T	XP_016883034.1:p.Gly1934=
XM_017027546.1:c.3330G>T	XP_016883035.1:p.Gly1110=
NM_014727.3:c.6366G>T MANE Select	NP_055542.1:p.Gly2122=