Canonical Allele Identifier: CA405419138

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36220969C>G (hg19) ; chr19:g.35730068C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35730068C>G , CM000681.2:g.35730068C>G	GRCh38
NC_000019.9:g.36220969C>G , CM000681.1:g.36220969C>G	GRCh37
NC_000019.8:g.40912809C>G	NCBI36
NG_052906.1:g.17050C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.4953C>G	ENSP00000501283.1:p.Ile1651Met
ENST00000674114.2:c.2560C>G	ENSP00000501039.2:n.2560C>G
ENST00000684977.1:c.237C>G	ENSP00000509384.1:p.Ile79Met
ENST00000685168.1:c.445C>G
ENST00000689544.1:n.172C>G
ENST00000691421.1:c.240C>G	ENSP00000508674.1:p.Ile80Met
ENST00000691855.1:c.4561C>G
ENST00000692961.1:c.5019C>G	ENSP00000509289.1:p.Ile1673Met
ENST00000420124.4:c.5019C>G MANE Select	ENSP00000398837.2:p.Ile1673Met
ENST00000673918.1:c.4953C>G	ENSP00000501283.1:p.Ile1651Met
ENST00000674114.1:c.2341C>G
ENST00000420124.2:c.5019C>G	ENSP00000398837.1:p.Ile1673Met
NM_014727.2:c.5019C>G	NP_055542.1:p.Ile1673Met
XM_011527561.1:c.4953C>G	XP_011525863.1:p.Ile1651Met
XM_011527562.1:c.5019C>G	XP_011525864.1:p.Ile1673Met
XM_011527563.1:c.4743C>G	XP_011525865.1:p.Ile1581Met
XM_011527561.2:c.4455C>G	XP_011525863.2:p.Ile1485Met
XM_011527562.2:c.5019C>G	XP_011525864.1:p.Ile1673Met
XM_017027544.1:c.5019C>G	XP_016883033.1:p.Ile1673Met
XM_017027545.1:c.4455C>G	XP_016883034.1:p.Ile1485Met
XM_017027546.1:c.1983C>G	XP_016883035.1:p.Ile661Met
NM_014727.3:c.5019C>G MANE Select	NP_055542.1:p.Ile1673Met