Canonical Allele Identifier: CA507072696

Gene: KMT2B

Linked Data

• gnomAD v4: 19-35730114-C-T
• MyVariant Identifiers: chr19:g.36221015C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35730114C>T , CM000681.2:g.35730114C>T	GRCh38
NC_000019.9:g.36221015C>T , CM000681.1:g.36221015C>T	GRCh37
NC_000019.8:g.40912855C>T	NCBI36
NG_052906.1:g.17096C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.4999C>T	ENSP00000501283.1:p.Leu1667=
ENST00000674114.2:c.2606C>T	ENSP00000501039.2:n.2606C>T
ENST00000684977.1:c.283C>T	ENSP00000509384.1:p.Leu95=
ENST00000685168.1:c.491C>T
ENST00000689544.1:n.218C>T
ENST00000691421.1:c.286C>T	ENSP00000508674.1:p.Leu96=
ENST00000691855.1:c.4607C>T
ENST00000692961.1:c.5065C>T	ENSP00000509289.1:p.Leu1689=
ENST00000420124.4:c.5065C>T MANE Select	ENSP00000398837.2:p.Leu1689=
ENST00000673918.1:c.4999C>T	ENSP00000501283.1:p.Leu1667=
ENST00000674114.1:c.2387C>T
ENST00000420124.2:c.5065C>T	ENSP00000398837.1:p.Leu1689=
NM_014727.2:c.5065C>T	NP_055542.1:p.Leu1689=
XM_011527561.1:c.4999C>T	XP_011525863.1:p.Leu1667=
XM_011527562.1:c.5065C>T	XP_011525864.1:p.Leu1689=
XM_011527563.1:c.4789C>T	XP_011525865.1:p.Leu1597=
XM_011527561.2:c.4501C>T	XP_011525863.2:p.Leu1501=
XM_011527562.2:c.5065C>T	XP_011525864.1:p.Leu1689=
XM_017027544.1:c.5065C>T	XP_016883033.1:p.Leu1689=
XM_017027545.1:c.4501C>T	XP_016883034.1:p.Leu1501=
XM_017027546.1:c.2029C>T	XP_016883035.1:p.Leu677=
NM_014727.3:c.5065C>T MANE Select	NP_055542.1:p.Leu1689=