Canonical Allele Identifier: CA507309093

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36223927C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35733026C>G , CM000681.2:g.35733026C>G	GRCh38
NC_000019.9:g.36223927C>G , CM000681.1:g.36223927C>G	GRCh37
NC_000019.8:g.40915767C>G	NCBI36
NG_052906.1:g.20008C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.783C>G
ENST00000673918.2:c.6411C>G	ENSP00000501283.1:p.Pro2137=
ENST00000674114.2:c.4018C>G	ENSP00000501039.2:n.4018C>G
ENST00000684977.1:c.1695C>G	ENSP00000509384.1:p.Pro565=
ENST00000689544.1:n.1630C>G
ENST00000691421.1:c.1698C>G	ENSP00000508674.1:p.Pro566=
ENST00000691855.1:c.6019C>G
ENST00000692961.1:c.6477C>G	ENSP00000509289.1:p.Pro2159=
ENST00000693677.1:c.705-571C>G	ENSP00000509779.1:n.705-571C>G
ENST00000420124.4:c.6477C>G MANE Select	ENSP00000398837.2:p.Pro2159=
ENST00000673918.1:c.6411C>G	ENSP00000501283.1:p.Pro2137=
ENST00000674114.1:c.3799C>G
ENST00000420124.2:c.6477C>G	ENSP00000398837.1:p.Pro2159=
NM_014727.2:c.6477C>G	NP_055542.1:p.Pro2159=
XM_011527561.1:c.6411C>G	XP_011525863.1:p.Pro2137=
XM_011527562.1:c.6477C>G	XP_011525864.1:p.Pro2159=
XM_011527563.1:c.6201C>G	XP_011525865.1:p.Pro2067=
XM_011527561.2:c.5913C>G	XP_011525863.2:p.Pro1971=
XM_011527562.2:c.6477C>G	XP_011525864.1:p.Pro2159=
XM_017027544.1:c.6477C>G	XP_016883033.1:p.Pro2159=
XM_017027545.1:c.5913C>G	XP_016883034.1:p.Pro1971=
XM_017027546.1:c.3441C>G	XP_016883035.1:p.Pro1147=
NM_014727.3:c.6477C>G MANE Select	NP_055542.1:p.Pro2159=