Canonical Allele Identifier: CA995473470
Gene: KMT2B HGNC NCBI

Linked Data

dbSNP Id: rs1969621505

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35729845_35729861dup , CM000681.2:g.35729845_35729861dup GRCh38
NC_000019.9:g.36220746_36220762dup , CM000681.1:g.36220746_36220762dup GRCh37
NC_000019.8:g.40912586_40912602dup NCBI36
NG_052906.1:g.16827_16843dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000673918.2:c.4852-122_4852-106dup ENSP00000501283.1:n.4852-122_4852-106dup
ENST00000674114.2:c.2459-122_2459-106dup ENSP00000501039.2:n.2459-122_2459-106dup
ENST00000684977.1:c.136-122_136-106dup ENSP00000509384.1:n.136-122_136-106dup
ENST00000685168.1:c.344-122_344-106dup
ENST00000689544.1:n.71-122_71-106dup
ENST00000691421.1:c.139-122_139-106dup ENSP00000508674.1:n.139-122_139-106dup
ENST00000691855.1:c.4460-122_4460-106dup
ENST00000692961.1:c.4918-122_4918-106dup ENSP00000509289.1:n.4918-122_4918-106dup
ENST00000420124.4:c.4918-122_4918-106dup MANE Select ENSP00000398837.2:n.4918-122_4918-106dup
ENST00000673918.1:c.4852-122_4852-106dup ENSP00000501283.1:n.4852-122_4852-106dup
ENST00000674114.1:c.2240-122_2240-106dup
ENST00000420124.2:c.4918-122_4918-106dup ENSP00000398837.1:n.4918-122_4918-106dup
NM_014727.2:c.4918-122_4918-106dup NP_055542.1:n.4918-122_4918-106dup
XM_011527561.1:c.4852-122_4852-106dup XP_011525863.1:n.4852-122_4852-106dup
XM_011527562.1:c.4918-122_4918-106dup XP_011525864.1:n.4918-122_4918-106dup
XM_011527563.1:c.4642-122_4642-106dup XP_011525865.1:n.4642-122_4642-106dup
XM_011527561.2:c.4354-122_4354-106dup XP_011525863.2:n.4354-122_4354-106dup
XM_011527562.2:c.4918-122_4918-106dup XP_011525864.1:n.4918-122_4918-106dup
XM_017027544.1:c.4918-122_4918-106dup XP_016883033.1:n.4918-122_4918-106dup
XM_017027545.1:c.4354-122_4354-106dup XP_016883034.1:n.4354-122_4354-106dup
XM_017027546.1:c.1882-122_1882-106dup XP_016883035.1:n.1882-122_1882-106dup
NM_014727.3:c.4918-122_4918-106dup MANE Select NP_055542.1:n.4918-122_4918-106dup