Canonical Allele Identifier: CA405428814

Gene: KMT2B

Linked Data

• gnomAD v4: 19-35733036-T-G
• MyVariant Identifiers: chr19:g.36223937T>G (hg19) ; chr19:g.35733036T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35733036T>G , CM000681.2:g.35733036T>G	GRCh38
NC_000019.9:g.36223937T>G , CM000681.1:g.36223937T>G	GRCh37
NC_000019.8:g.40915777T>G	NCBI36
NG_052906.1:g.20018T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.793T>G
ENST00000673918.2:c.6421T>G	ENSP00000501283.1:p.Phe2141Val
ENST00000674114.2:c.4028T>G	ENSP00000501039.2:n.4028T>G
ENST00000684977.1:c.1705T>G	ENSP00000509384.1:p.Phe569Val
ENST00000689544.1:n.1640T>G
ENST00000691421.1:c.1708T>G	ENSP00000508674.1:p.Phe570Val
ENST00000691855.1:c.6029T>G
ENST00000692961.1:c.6487T>G	ENSP00000509289.1:p.Phe2163Val
ENST00000693677.1:c.705-561T>G	ENSP00000509779.1:n.705-561T>G
ENST00000420124.4:c.6487T>G MANE Select	ENSP00000398837.2:p.Phe2163Val
ENST00000673918.1:c.6421T>G	ENSP00000501283.1:p.Phe2141Val
ENST00000674114.1:c.3809T>G
ENST00000420124.2:c.6487T>G	ENSP00000398837.1:p.Phe2163Val
NM_014727.2:c.6487T>G	NP_055542.1:p.Phe2163Val
XM_011527561.1:c.6421T>G	XP_011525863.1:p.Phe2141Val
XM_011527562.1:c.6487T>G	XP_011525864.1:p.Phe2163Val
XM_011527563.1:c.6211T>G	XP_011525865.1:p.Phe2071Val
XM_011527561.2:c.5923T>G	XP_011525863.2:p.Phe1975Val
XM_011527562.2:c.6487T>G	XP_011525864.1:p.Phe2163Val
XM_017027544.1:c.6487T>G	XP_016883033.1:p.Phe2163Val
XM_017027545.1:c.5923T>G	XP_016883034.1:p.Phe1975Val
XM_017027546.1:c.3451T>G	XP_016883035.1:p.Phe1151Val
NM_014727.3:c.6487T>G MANE Select	NP_055542.1:p.Phe2163Val