Canonical Allele Identifier: CA507308110

Gene: KMT2B

Linked Data

• dbSNP Id: rs1334250525
• gnomAD v2: 19-36223421-C-T
• MyVariant Identifiers: chr19:g.36223421C>T (hg19) ; chr19:g.35732520C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732520C>T , CM000681.2:g.35732520C>T	GRCh38
NC_000019.9:g.36223421C>T , CM000681.1:g.36223421C>T	GRCh37
NC_000019.8:g.40915261C>T	NCBI36
NG_052906.1:g.19502C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.277C>T
ENST00000673918.2:c.5905C>T	ENSP00000501283.1:p.Leu1969=
ENST00000674114.2:c.3512C>T	ENSP00000501039.2:n.3512C>T
ENST00000684977.1:c.1189C>T	ENSP00000509384.1:p.Leu397=
ENST00000689544.1:n.1124C>T
ENST00000691421.1:c.1192C>T	ENSP00000508674.1:p.Leu398=
ENST00000691855.1:c.5513C>T
ENST00000692961.1:c.5971C>T	ENSP00000509289.1:p.Leu1991=
ENST00000693677.1:c.704+191C>T	ENSP00000509779.1:n.704+191C>T
ENST00000420124.4:c.5971C>T MANE Select	ENSP00000398837.2:p.Leu1991=
ENST00000673918.1:c.5905C>T	ENSP00000501283.1:p.Leu1969=
ENST00000674114.1:c.3293C>T
ENST00000420124.2:c.5971C>T	ENSP00000398837.1:p.Leu1991=
NM_014727.2:c.5971C>T	NP_055542.1:p.Leu1991=
XM_011527561.1:c.5905C>T	XP_011525863.1:p.Leu1969=
XM_011527562.1:c.5971C>T	XP_011525864.1:p.Leu1991=
XM_011527563.1:c.5695C>T	XP_011525865.1:p.Leu1899=
XM_011527561.2:c.5407C>T	XP_011525863.2:p.Leu1803=
XM_011527562.2:c.5971C>T	XP_011525864.1:p.Leu1991=
XM_017027544.1:c.5971C>T	XP_016883033.1:p.Leu1991=
XM_017027545.1:c.5407C>T	XP_016883034.1:p.Leu1803=
XM_017027546.1:c.2935C>T	XP_016883035.1:p.Leu979=
NM_014727.3:c.5971C>T MANE Select	NP_055542.1:p.Leu1991=