Canonical Allele Identifier: CA405419147

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36220970T>G (hg19) ; chr19:g.35730069T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35730069T>G , CM000681.2:g.35730069T>G	GRCh38
NC_000019.9:g.36220970T>G , CM000681.1:g.36220970T>G	GRCh37
NC_000019.8:g.40912810T>G	NCBI36
NG_052906.1:g.17051T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.4954T>G	ENSP00000501283.1:p.Phe1652Val
ENST00000674114.2:c.2561T>G	ENSP00000501039.2:n.2561T>G
ENST00000684977.1:c.238T>G	ENSP00000509384.1:p.Phe80Val
ENST00000685168.1:c.446T>G
ENST00000689544.1:n.173T>G
ENST00000691421.1:c.241T>G	ENSP00000508674.1:p.Phe81Val
ENST00000691855.1:c.4562T>G
ENST00000692961.1:c.5020T>G	ENSP00000509289.1:p.Phe1674Val
ENST00000420124.4:c.5020T>G MANE Select	ENSP00000398837.2:p.Phe1674Val
ENST00000673918.1:c.4954T>G	ENSP00000501283.1:p.Phe1652Val
ENST00000674114.1:c.2342T>G
ENST00000420124.2:c.5020T>G	ENSP00000398837.1:p.Phe1674Val
NM_014727.2:c.5020T>G	NP_055542.1:p.Phe1674Val
XM_011527561.1:c.4954T>G	XP_011525863.1:p.Phe1652Val
XM_011527562.1:c.5020T>G	XP_011525864.1:p.Phe1674Val
XM_011527563.1:c.4744T>G	XP_011525865.1:p.Phe1582Val
XM_011527561.2:c.4456T>G	XP_011525863.2:p.Phe1486Val
XM_011527562.2:c.5020T>G	XP_011525864.1:p.Phe1674Val
XM_017027544.1:c.5020T>G	XP_016883033.1:p.Phe1674Val
XM_017027545.1:c.4456T>G	XP_016883034.1:p.Phe1486Val
XM_017027546.1:c.1984T>G	XP_016883035.1:p.Phe662Val
NM_014727.3:c.5020T>G MANE Select	NP_055542.1:p.Phe1674Val