Canonical Allele Identifier: CA405425076

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36223449C>G (hg19) ; chr19:g.35732548C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732548C>G , CM000681.2:g.35732548C>G	GRCh38
NC_000019.9:g.36223449C>G , CM000681.1:g.36223449C>G	GRCh37
NC_000019.8:g.40915289C>G	NCBI36
NG_052906.1:g.19530C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.305C>G
ENST00000673918.2:c.5933C>G	ENSP00000501283.1:p.Thr1978Ser
ENST00000674114.2:c.3540C>G	ENSP00000501039.2:n.3540C>G
ENST00000684977.1:c.1217C>G	ENSP00000509384.1:p.Thr406Ser
ENST00000689544.1:n.1152C>G
ENST00000691421.1:c.1220C>G	ENSP00000508674.1:p.Thr407Ser
ENST00000691855.1:c.5541C>G
ENST00000692961.1:c.5999C>G	ENSP00000509289.1:p.Thr2000Ser
ENST00000693677.1:c.704+219C>G	ENSP00000509779.1:n.704+219C>G
ENST00000420124.4:c.5999C>G MANE Select	ENSP00000398837.2:p.Thr2000Ser
ENST00000673918.1:c.5933C>G	ENSP00000501283.1:p.Thr1978Ser
ENST00000674114.1:c.3321C>G
ENST00000420124.2:c.5999C>G	ENSP00000398837.1:p.Thr2000Ser
NM_014727.2:c.5999C>G	NP_055542.1:p.Thr2000Ser
XM_011527561.1:c.5933C>G	XP_011525863.1:p.Thr1978Ser
XM_011527562.1:c.5999C>G	XP_011525864.1:p.Thr2000Ser
XM_011527563.1:c.5723C>G	XP_011525865.1:p.Thr1908Ser
XM_011527561.2:c.5435C>G	XP_011525863.2:p.Thr1812Ser
XM_011527562.2:c.5999C>G	XP_011525864.1:p.Thr2000Ser
XM_017027544.1:c.5999C>G	XP_016883033.1:p.Thr2000Ser
XM_017027545.1:c.5435C>G	XP_016883034.1:p.Thr1812Ser
XM_017027546.1:c.2963C>G	XP_016883035.1:p.Thr988Ser
NM_014727.3:c.5999C>G MANE Select	NP_055542.1:p.Thr2000Ser