Canonical Allele Identifier: CA2333795032
Gene: KMT2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35733765C= , CM000681.2:g.35733765C= GRCh38
NC_000019.9:g.36224666C= , CM000681.1:g.36224666C= GRCh37
NC_000019.8:g.40916506C= NCBI36
NG_052906.1:g.20747C=

Transcript Alleles

HGVS Amino-acid change
ENST00000592092.2:n.1522C=
ENST00000673918.2:c.6986C= ENSP00000501283.1:p.Pro2329=
ENST00000674114.2:c.4593C= ENSP00000501039.2:n.4593C=
ENST00000684977.1:c.2247C= ENSP00000509384.1:n.2247C=
ENST00000689544.1:n.2293C=
ENST00000689929.1:c.3C=
ENST00000691421.1:c.2183C= ENSP00000508674.1:p.Pro728=
ENST00000691855.1:c.6594C=
ENST00000692961.1:c.6976C= ENSP00000509289.1:p.Pro2326=
ENST00000693175.1:c.3C=
ENST00000693677.1:c.797C= ENSP00000509779.1:p.Pro266=
ENST00000420124.4:c.7052C= MANE Select ENSP00000398837.2:p.Pro2351=
ENST00000673918.1:c.6986C= ENSP00000501283.1:p.Pro2329=
ENST00000674114.1:c.4374C=
ENST00000420124.2:c.7052C= ENSP00000398837.1:p.Pro2351=
ENST00000592092.1:n.432C=
NM_014727.2:c.7052C= NP_055542.1:p.Pro2351=
XM_011527561.1:c.6986C= XP_011525863.1:p.Pro2329=
XM_011527562.1:c.7052C= XP_011525864.1:p.Pro2351=
XM_011527563.1:c.6776C= XP_011525865.1:p.Pro2259=
XM_011527561.2:c.6488C= XP_011525863.2:p.Pro2163=
XM_011527562.2:c.7052C= XP_011525864.1:p.Pro2351=
XM_017027544.1:c.6962C= XP_016883033.1:p.Pro2321=
XM_017027545.1:c.6488C= XP_016883034.1:p.Pro2163=
XM_017027546.1:c.4016C= XP_016883035.1:p.Pro1339=
NM_014727.3:c.7052C= MANE Select NP_055542.1:p.Pro2351=