Canonical Allele Identifier: CA1879478398

Gene: LMX1B

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.126693150G= , CM000671.2:g.126693150G=	GRCh38
NC_000009.11:g.129455429G= , CM000671.1:g.129455429G=	GRCh37
NC_000009.10:g.128495250G=	NCBI36
NG_017039.1:g.83708G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355497.10:c.568G=	ENSP00000347684.5:p.Glu190=
ENST00000373474.9:c.568G= MANE Select	ENSP00000362573.3:p.Glu190=
ENST00000526117.6:c.568G=	ENSP00000436930.1:p.Glu190=
ENST00000355497.9:c.568G=	ENSP00000347684.5:p.Glu190=
ENST00000373474.8:c.568G=	ENSP00000362573.3:p.Glu190=
ENST00000526117.5:c.568G=	ENSP00000436930.1:p.Glu190=
ENST00000561065.1:c.499G=	ENSP00000453580.1:p.Glu167=
NM_001174146.1:c.568G=	NP_001167617.1:p.Glu190=
NM_001174147.1:c.568G=	NP_001167618.1:p.Glu190=
NM_002316.3:c.568G=	NP_002307.2:p.Glu190=
NM_001174146.2:c.568G=	NP_001167617.1:p.Glu190=
NM_001174147.2:c.568G= MANE Select	NP_001167618.1:p.Glu190=
NM_002316.4:c.568G=	NP_002307.2:p.Glu190=