Canonical Allele Identifier: CA507308676
Gene: KMT2B HGNC NCBI

Linked Data

dbSNP Id: rs1969767338
MyVariant Identifiers: chr19:g.36223811C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35732910C>T , CM000681.2:g.35732910C>T GRCh38
NC_000019.9:g.36223811C>T , CM000681.1:g.36223811C>T GRCh37
NC_000019.8:g.40915651C>T NCBI36
NG_052906.1:g.19892C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000592092.2:n.667C>T
ENST00000673918.2:c.6295C>T ENSP00000501283.1:p.Leu2099=
ENST00000674114.2:c.3902C>T ENSP00000501039.2:n.3902C>T
ENST00000684977.1:c.1579C>T ENSP00000509384.1:p.Leu527=
ENST00000689544.1:n.1514C>T
ENST00000691421.1:c.1582C>T ENSP00000508674.1:p.Leu528=
ENST00000691855.1:c.5903C>T
ENST00000692961.1:c.6361C>T ENSP00000509289.1:p.Leu2121=
ENST00000693677.1:c.704+581C>T ENSP00000509779.1:n.704+581C>T
ENST00000420124.4:c.6361C>T MANE Select ENSP00000398837.2:p.Leu2121=
ENST00000673918.1:c.6295C>T ENSP00000501283.1:p.Leu2099=
ENST00000674114.1:c.3683C>T
ENST00000420124.2:c.6361C>T ENSP00000398837.1:p.Leu2121=
NM_014727.2:c.6361C>T NP_055542.1:p.Leu2121=
XM_011527561.1:c.6295C>T XP_011525863.1:p.Leu2099=
XM_011527562.1:c.6361C>T XP_011525864.1:p.Leu2121=
XM_011527563.1:c.6085C>T XP_011525865.1:p.Leu2029=
XM_011527561.2:c.5797C>T XP_011525863.2:p.Leu1933=
XM_011527562.2:c.6361C>T XP_011525864.1:p.Leu2121=
XM_017027544.1:c.6361C>T XP_016883033.1:p.Leu2121=
XM_017027545.1:c.5797C>T XP_016883034.1:p.Leu1933=
XM_017027546.1:c.3325C>T XP_016883035.1:p.Leu1109=
NM_014727.3:c.6361C>T MANE Select NP_055542.1:p.Leu2121=