Canonical Allele Identifier: CA405419336

Gene: KMT2B

Linked Data

• dbSNP Id: rs1969632594
• MyVariant Identifiers: chr19:g.36221012C>G (hg19) ; chr19:g.35730111C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35730111C>G , CM000681.2:g.35730111C>G	GRCh38
NC_000019.9:g.36221012C>G , CM000681.1:g.36221012C>G	GRCh37
NC_000019.8:g.40912852C>G	NCBI36
NG_052906.1:g.17093C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.4996C>G	ENSP00000501283.1:p.Leu1666Val
ENST00000674114.2:c.2603C>G	ENSP00000501039.2:n.2603C>G
ENST00000684977.1:c.280C>G	ENSP00000509384.1:p.Leu94Val
ENST00000685168.1:c.488C>G
ENST00000689544.1:n.215C>G
ENST00000691421.1:c.283C>G	ENSP00000508674.1:p.Leu95Val
ENST00000691855.1:c.4604C>G
ENST00000692961.1:c.5062C>G	ENSP00000509289.1:p.Leu1688Val
ENST00000420124.4:c.5062C>G MANE Select	ENSP00000398837.2:p.Leu1688Val
ENST00000673918.1:c.4996C>G	ENSP00000501283.1:p.Leu1666Val
ENST00000674114.1:c.2384C>G
ENST00000420124.2:c.5062C>G	ENSP00000398837.1:p.Leu1688Val
NM_014727.2:c.5062C>G	NP_055542.1:p.Leu1688Val
XM_011527561.1:c.4996C>G	XP_011525863.1:p.Leu1666Val
XM_011527562.1:c.5062C>G	XP_011525864.1:p.Leu1688Val
XM_011527563.1:c.4786C>G	XP_011525865.1:p.Leu1596Val
XM_011527561.2:c.4498C>G	XP_011525863.2:p.Leu1500Val
XM_011527562.2:c.5062C>G	XP_011525864.1:p.Leu1688Val
XM_017027544.1:c.5062C>G	XP_016883033.1:p.Leu1688Val
XM_017027545.1:c.4498C>G	XP_016883034.1:p.Leu1500Val
XM_017027546.1:c.2026C>G	XP_016883035.1:p.Leu676Val
NM_014727.3:c.5062C>G MANE Select	NP_055542.1:p.Leu1688Val