Canonical Allele Identifier: CA507072595

Gene: KMT2B

Linked Data

• gnomAD v4: 19-35730029-C-T
• MyVariant Identifiers: chr19:g.36220930C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35730029C>T , CM000681.2:g.35730029C>T	GRCh38
NC_000019.9:g.36220930C>T , CM000681.1:g.36220930C>T	GRCh37
NC_000019.8:g.40912770C>T	NCBI36
NG_052906.1:g.17011C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.4914C>T	ENSP00000501283.1:p.Ser1638=
ENST00000674114.2:c.2521C>T	ENSP00000501039.2:n.2521C>T
ENST00000684977.1:c.198C>T	ENSP00000509384.1:p.Ser66=
ENST00000685168.1:c.406C>T
ENST00000689544.1:n.133C>T
ENST00000691421.1:c.201C>T	ENSP00000508674.1:p.Ser67=
ENST00000691855.1:c.4522C>T
ENST00000692961.1:c.4980C>T	ENSP00000509289.1:p.Ser1660=
ENST00000420124.4:c.4980C>T MANE Select	ENSP00000398837.2:p.Ser1660=
ENST00000673918.1:c.4914C>T	ENSP00000501283.1:p.Ser1638=
ENST00000674114.1:c.2302C>T
ENST00000420124.2:c.4980C>T	ENSP00000398837.1:p.Ser1660=
NM_014727.2:c.4980C>T	NP_055542.1:p.Ser1660=
XM_011527561.1:c.4914C>T	XP_011525863.1:p.Ser1638=
XM_011527562.1:c.4980C>T	XP_011525864.1:p.Ser1660=
XM_011527563.1:c.4704C>T	XP_011525865.1:p.Ser1568=
XM_011527561.2:c.4416C>T	XP_011525863.2:p.Ser1472=
XM_011527562.2:c.4980C>T	XP_011525864.1:p.Ser1660=
XM_017027544.1:c.4980C>T	XP_016883033.1:p.Ser1660=
XM_017027545.1:c.4416C>T	XP_016883034.1:p.Ser1472=
XM_017027546.1:c.1944C>T	XP_016883035.1:p.Ser648=
NM_014727.3:c.4980C>T MANE Select	NP_055542.1:p.Ser1660=