Canonical Allele Identifier: CA507308806
Gene: KMT2B HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.36224673G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35733772G>A , CM000681.2:g.35733772G>A GRCh38
NC_000019.9:g.36224673G>A , CM000681.1:g.36224673G>A GRCh37
NC_000019.8:g.40916513G>A NCBI36
NG_052906.1:g.20754G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000592092.2:n.1529G>A
ENST00000673918.2:c.6993G>A ENSP00000501283.1:p.Gln2331=
ENST00000674114.2:c.4600G>A ENSP00000501039.2:n.4600G>A
ENST00000684977.1:c.2254G>A ENSP00000509384.1:n.2254G>A
ENST00000689544.1:n.2300G>A
ENST00000689929.1:c.10G>A
ENST00000691421.1:c.2190G>A ENSP00000508674.1:p.Gln730=
ENST00000691855.1:c.6601G>A
ENST00000692961.1:c.6983G>A ENSP00000509289.1:p.Arg2328Lys
ENST00000693175.1:c.10G>A
ENST00000693677.1:c.804G>A ENSP00000509779.1:p.Gln268=
ENST00000420124.4:c.7059G>A MANE Select ENSP00000398837.2:p.Gln2353=
ENST00000673918.1:c.6993G>A ENSP00000501283.1:p.Gln2331=
ENST00000674114.1:c.4381G>A
ENST00000420124.2:c.7059G>A ENSP00000398837.1:p.Gln2353=
ENST00000592092.1:n.439G>A
NM_014727.2:c.7059G>A NP_055542.1:p.Gln2353=
XM_011527561.1:c.6993G>A XP_011525863.1:p.Gln2331=
XM_011527562.1:c.7059G>A XP_011525864.1:p.Gln2353=
XM_011527563.1:c.6783G>A XP_011525865.1:p.Gln2261=
XM_011527561.2:c.6495G>A XP_011525863.2:p.Gln2165=
XM_011527562.2:c.7059G>A XP_011525864.1:p.Gln2353=
XM_017027544.1:c.6969G>A XP_016883033.1:p.Gln2323=
XM_017027545.1:c.6495G>A XP_016883034.1:p.Gln2165=
XM_017027546.1:c.4023G>A XP_016883035.1:p.Gln1341=
NM_014727.3:c.7059G>A MANE Select NP_055542.1:p.Gln2353=