Canonical Allele Identifier: CA405418923

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36220932A>C (hg19) ; chr19:g.35730031A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35730031A>C , CM000681.2:g.35730031A>C	GRCh38
NC_000019.9:g.36220932A>C , CM000681.1:g.36220932A>C	GRCh37
NC_000019.8:g.40912772A>C	NCBI36
NG_052906.1:g.17013A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.4916A>C	ENSP00000501283.1:p.Asn1639Thr
ENST00000674114.2:c.2523A>C	ENSP00000501039.2:n.2523A>C
ENST00000684977.1:c.200A>C	ENSP00000509384.1:p.Asn67Thr
ENST00000685168.1:c.408A>C
ENST00000689544.1:n.135A>C
ENST00000691421.1:c.203A>C	ENSP00000508674.1:p.Asn68Thr
ENST00000691855.1:c.4524A>C
ENST00000692961.1:c.4982A>C	ENSP00000509289.1:p.Asn1661Thr
ENST00000420124.4:c.4982A>C MANE Select	ENSP00000398837.2:p.Asn1661Thr
ENST00000673918.1:c.4916A>C	ENSP00000501283.1:p.Asn1639Thr
ENST00000674114.1:c.2304A>C
ENST00000420124.2:c.4982A>C	ENSP00000398837.1:p.Asn1661Thr
NM_014727.2:c.4982A>C	NP_055542.1:p.Asn1661Thr
XM_011527561.1:c.4916A>C	XP_011525863.1:p.Asn1639Thr
XM_011527562.1:c.4982A>C	XP_011525864.1:p.Asn1661Thr
XM_011527563.1:c.4706A>C	XP_011525865.1:p.Asn1569Thr
XM_011527561.2:c.4418A>C	XP_011525863.2:p.Asn1473Thr
XM_011527562.2:c.4982A>C	XP_011525864.1:p.Asn1661Thr
XM_017027544.1:c.4982A>C	XP_016883033.1:p.Asn1661Thr
XM_017027545.1:c.4418A>C	XP_016883034.1:p.Asn1473Thr
XM_017027546.1:c.1946A>C	XP_016883035.1:p.Asn649Thr
NM_014727.3:c.4982A>C MANE Select	NP_055542.1:p.Asn1661Thr