Canonical Allele Identifier: CA507308168

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36223439C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732538C>T , CM000681.2:g.35732538C>T	GRCh38
NC_000019.9:g.36223439C>T , CM000681.1:g.36223439C>T	GRCh37
NC_000019.8:g.40915279C>T	NCBI36
NG_052906.1:g.19520C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.295C>T
ENST00000673918.2:c.5923C>T	ENSP00000501283.1:p.Leu1975=
ENST00000674114.2:c.3530C>T	ENSP00000501039.2:n.3530C>T
ENST00000684977.1:c.1207C>T	ENSP00000509384.1:p.Leu403=
ENST00000689544.1:n.1142C>T
ENST00000691421.1:c.1210C>T	ENSP00000508674.1:p.Leu404=
ENST00000691855.1:c.5531C>T
ENST00000692961.1:c.5989C>T	ENSP00000509289.1:p.Leu1997=
ENST00000693677.1:c.704+209C>T	ENSP00000509779.1:n.704+209C>T
ENST00000420124.4:c.5989C>T MANE Select	ENSP00000398837.2:p.Leu1997=
ENST00000673918.1:c.5923C>T	ENSP00000501283.1:p.Leu1975=
ENST00000674114.1:c.3311C>T
ENST00000420124.2:c.5989C>T	ENSP00000398837.1:p.Leu1997=
NM_014727.2:c.5989C>T	NP_055542.1:p.Leu1997=
XM_011527561.1:c.5923C>T	XP_011525863.1:p.Leu1975=
XM_011527562.1:c.5989C>T	XP_011525864.1:p.Leu1997=
XM_011527563.1:c.5713C>T	XP_011525865.1:p.Leu1905=
XM_011527561.2:c.5425C>T	XP_011525863.2:p.Leu1809=
XM_011527562.2:c.5989C>T	XP_011525864.1:p.Leu1997=
XM_017027544.1:c.5989C>T	XP_016883033.1:p.Leu1997=
XM_017027545.1:c.5425C>T	XP_016883034.1:p.Leu1809=
XM_017027546.1:c.2953C>T	XP_016883035.1:p.Leu985=
NM_014727.3:c.5989C>T MANE Select	NP_055542.1:p.Leu1997=