Canonical Allele Identifier: CA405424734

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36223398T>G (hg19) ; chr19:g.35732497T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732497T>G , CM000681.2:g.35732497T>G	GRCh38
NC_000019.9:g.36223398T>G , CM000681.1:g.36223398T>G	GRCh37
NC_000019.8:g.40915238T>G	NCBI36
NG_052906.1:g.19479T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.254T>G
ENST00000673918.2:c.5882T>G	ENSP00000501283.1:p.Val1961Gly
ENST00000674114.2:c.3489T>G	ENSP00000501039.2:n.3489T>G
ENST00000684977.1:c.1166T>G	ENSP00000509384.1:p.Val389Gly
ENST00000689544.1:n.1101T>G
ENST00000691421.1:c.1169T>G	ENSP00000508674.1:p.Val390Gly
ENST00000691855.1:c.5490T>G
ENST00000692961.1:c.5948T>G	ENSP00000509289.1:p.Val1983Gly
ENST00000693677.1:c.704+168T>G	ENSP00000509779.1:n.704+168T>G
ENST00000420124.4:c.5948T>G MANE Select	ENSP00000398837.2:p.Val1983Gly
ENST00000673918.1:c.5882T>G	ENSP00000501283.1:p.Val1961Gly
ENST00000674114.1:c.3270T>G
ENST00000420124.2:c.5948T>G	ENSP00000398837.1:p.Val1983Gly
NM_014727.2:c.5948T>G	NP_055542.1:p.Val1983Gly
XM_011527561.1:c.5882T>G	XP_011525863.1:p.Val1961Gly
XM_011527562.1:c.5948T>G	XP_011525864.1:p.Val1983Gly
XM_011527563.1:c.5672T>G	XP_011525865.1:p.Val1891Gly
XM_011527561.2:c.5384T>G	XP_011525863.2:p.Val1795Gly
XM_011527562.2:c.5948T>G	XP_011525864.1:p.Val1983Gly
XM_017027544.1:c.5948T>G	XP_016883033.1:p.Val1983Gly
XM_017027545.1:c.5384T>G	XP_016883034.1:p.Val1795Gly
XM_017027546.1:c.2912T>G	XP_016883035.1:p.Val971Gly
NM_014727.3:c.5948T>G MANE Select	NP_055542.1:p.Val1983Gly