Canonical Allele Identifier: CA2333793073
Gene: KMT2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35729972C= , CM000681.2:g.35729972C= GRCh38
NC_000019.9:g.36220873C= , CM000681.1:g.36220873C= GRCh37
NC_000019.8:g.40912713C= NCBI36
NG_052906.1:g.16954C=

Transcript Alleles

HGVS Amino-acid change
ENST00000673918.2:c.4857C= ENSP00000501283.1:p.Cys1619=
ENST00000674114.2:c.2464C= ENSP00000501039.2:n.2464C=
ENST00000684977.1:c.141C= ENSP00000509384.1:p.Cys47=
ENST00000685168.1:c.349C=
ENST00000689544.1:n.76C=
ENST00000691421.1:c.144C= ENSP00000508674.1:p.Cys48=
ENST00000691855.1:c.4465C=
ENST00000692961.1:c.4923C= ENSP00000509289.1:p.Cys1641=
ENST00000420124.4:c.4923C= MANE Select ENSP00000398837.2:p.Cys1641=
ENST00000673918.1:c.4857C= ENSP00000501283.1:p.Cys1619=
ENST00000674114.1:c.2245C=
ENST00000420124.2:c.4923C= ENSP00000398837.1:p.Cys1641=
NM_014727.2:c.4923C= NP_055542.1:p.Cys1641=
XM_011527561.1:c.4857C= XP_011525863.1:p.Cys1619=
XM_011527562.1:c.4923C= XP_011525864.1:p.Cys1641=
XM_011527563.1:c.4647C= XP_011525865.1:p.Cys1549=
XM_011527561.2:c.4359C= XP_011525863.2:p.Cys1453=
XM_011527562.2:c.4923C= XP_011525864.1:p.Cys1641=
XM_017027544.1:c.4923C= XP_016883033.1:p.Cys1641=
XM_017027545.1:c.4359C= XP_016883034.1:p.Cys1453=
XM_017027546.1:c.1887C= XP_016883035.1:p.Cys629=
NM_014727.3:c.4923C= MANE Select NP_055542.1:p.Cys1641=