Canonical Allele Identifier: CA507072692

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36221008T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35730107T>C , CM000681.2:g.35730107T>C	GRCh38
NC_000019.9:g.36221008T>C , CM000681.1:g.36221008T>C	GRCh37
NC_000019.8:g.40912848T>C	NCBI36
NG_052906.1:g.17089T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.4992T>C	ENSP00000501283.1:p.Thr1664=
ENST00000674114.2:c.2599T>C	ENSP00000501039.2:n.2599T>C
ENST00000684977.1:c.276T>C	ENSP00000509384.1:p.Thr92=
ENST00000685168.1:c.484T>C
ENST00000689544.1:n.211T>C
ENST00000691421.1:c.279T>C	ENSP00000508674.1:p.Thr93=
ENST00000691855.1:c.4600T>C
ENST00000692961.1:c.5058T>C	ENSP00000509289.1:p.Thr1686=
ENST00000420124.4:c.5058T>C MANE Select	ENSP00000398837.2:p.Thr1686=
ENST00000673918.1:c.4992T>C	ENSP00000501283.1:p.Thr1664=
ENST00000674114.1:c.2380T>C
ENST00000420124.2:c.5058T>C	ENSP00000398837.1:p.Thr1686=
NM_014727.2:c.5058T>C	NP_055542.1:p.Thr1686=
XM_011527561.1:c.4992T>C	XP_011525863.1:p.Thr1664=
XM_011527562.1:c.5058T>C	XP_011525864.1:p.Thr1686=
XM_011527563.1:c.4782T>C	XP_011525865.1:p.Thr1594=
XM_011527561.2:c.4494T>C	XP_011525863.2:p.Thr1498=
XM_011527562.2:c.5058T>C	XP_011525864.1:p.Thr1686=
XM_017027544.1:c.5058T>C	XP_016883033.1:p.Thr1686=
XM_017027545.1:c.4494T>C	XP_016883034.1:p.Thr1498=
XM_017027546.1:c.2022T>C	XP_016883035.1:p.Thr674=
NM_014727.3:c.5058T>C MANE Select	NP_055542.1:p.Thr1686=