Canonical Allele Identifier: CA2584575161

Gene: KMT2B

Linked Data

• gnomAD v4: 19-35732802-CCTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732804_35732806del , CM000681.2:g.35732804_35732806del	GRCh38
NC_000019.9:g.36223705_36223707del , CM000681.1:g.36223705_36223707del	GRCh37
NC_000019.8:g.40915545_40915547del	NCBI36
NG_052906.1:g.19786_19788del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.561_563del
ENST00000673918.2:c.6189_6191del	ENSP00000501283.1:p.Ser2064del
ENST00000674114.2:c.3796_3798del	ENSP00000501039.2:n.3796_3798del
ENST00000684977.1:c.1473_1475del	ENSP00000509384.1:p.Ser492del
ENST00000689544.1:n.1408_1410del
ENST00000691421.1:c.1476_1478del	ENSP00000508674.1:p.Ser493del
ENST00000691855.1:c.5797_5799del
ENST00000692961.1:c.6255_6257del	ENSP00000509289.1:p.Ser2086del
ENST00000693677.1:c.704+475_704+477del	ENSP00000509779.1:n.704+475_704+477del
ENST00000420124.4:c.6255_6257del MANE Select	ENSP00000398837.2:p.Ser2086del
ENST00000673918.1:c.6189_6191del	ENSP00000501283.1:p.Ser2064del
ENST00000674114.1:c.3577_3579del
ENST00000420124.2:c.6255_6257del	ENSP00000398837.1:p.Ser2086del
NM_014727.2:c.6255_6257del	NP_055542.1:p.Ser2086del
XM_011527561.1:c.6189_6191del	XP_011525863.1:p.Ser2064del
XM_011527562.1:c.6255_6257del	XP_011525864.1:p.Ser2086del
XM_011527563.1:c.5979_5981del	XP_011525865.1:p.Ser1994del
XM_011527561.2:c.5691_5693del	XP_011525863.2:p.Ser1898del
XM_011527562.2:c.6255_6257del	XP_011525864.1:p.Ser2086del
XM_017027544.1:c.6255_6257del	XP_016883033.1:p.Ser2086del
XM_017027545.1:c.5691_5693del	XP_016883034.1:p.Ser1898del
XM_017027546.1:c.3219_3221del	XP_016883035.1:p.Ser1074del
NM_014727.3:c.6255_6257del MANE Select	NP_055542.1:p.Ser2086del