Canonical Allele Identifier: CA507308890

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36224092A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35733191A>T , CM000681.2:g.35733191A>T	GRCh38
NC_000019.9:g.36224092A>T , CM000681.1:g.36224092A>T	GRCh37
NC_000019.8:g.40915932A>T	NCBI36
NG_052906.1:g.20173A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.948A>T
ENST00000673918.2:c.6576A>T	ENSP00000501283.1:p.Pro2192=
ENST00000674114.2:c.4183A>T	ENSP00000501039.2:n.4183A>T
ENST00000684977.1:c.1860A>T	ENSP00000509384.1:p.Pro620=
ENST00000689544.1:n.1795A>T
ENST00000691421.1:c.1863A>T	ENSP00000508674.1:p.Pro621=
ENST00000691855.1:c.6184A>T
ENST00000692961.1:c.6642A>T	ENSP00000509289.1:p.Pro2214=
ENST00000693677.1:c.705-406A>T	ENSP00000509779.1:n.705-406A>T
ENST00000420124.4:c.6642A>T MANE Select	ENSP00000398837.2:p.Pro2214=
ENST00000673918.1:c.6576A>T	ENSP00000501283.1:p.Pro2192=
ENST00000674114.1:c.3964A>T
ENST00000420124.2:c.6642A>T	ENSP00000398837.1:p.Pro2214=
NM_014727.2:c.6642A>T	NP_055542.1:p.Pro2214=
XM_011527561.1:c.6576A>T	XP_011525863.1:p.Pro2192=
XM_011527562.1:c.6642A>T	XP_011525864.1:p.Pro2214=
XM_011527563.1:c.6366A>T	XP_011525865.1:p.Pro2122=
XM_011527561.2:c.6078A>T	XP_011525863.2:p.Pro2026=
XM_011527562.2:c.6642A>T	XP_011525864.1:p.Pro2214=
XM_017027544.1:c.6642A>T	XP_016883033.1:p.Pro2214=
XM_017027545.1:c.6078A>T	XP_016883034.1:p.Pro2026=
XM_017027546.1:c.3606A>T	XP_016883035.1:p.Pro1202=
NM_014727.3:c.6642A>T MANE Select	NP_055542.1:p.Pro2214=