Canonical Allele Identifier: CA1879436196

Gene: LMX1B

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.126615519C= , CM000671.2:g.126615519C=	GRCh38
NC_000009.11:g.129377798C= , CM000671.1:g.129377798C=	GRCh37
NC_000009.10:g.128417619C=	NCBI36
NG_017039.1:g.6077C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355497.10:c.276C=	ENSP00000347684.5:p.Thr92=
ENST00000373474.9:c.276C= MANE Select	ENSP00000362573.3:p.Thr92=
ENST00000526117.6:c.276C=	ENSP00000436930.1:p.Thr92=
ENST00000355497.9:c.276C=	ENSP00000347684.5:p.Thr92=
ENST00000373474.8:c.276C=	ENSP00000362573.3:p.Thr92=
ENST00000526117.5:c.276C=	ENSP00000436930.1:p.Thr92=
ENST00000561065.1:c.207C=	ENSP00000453580.1:p.Thr69=
NM_001174146.1:c.276C=	NP_001167617.1:p.Thr92=
NM_001174147.1:c.276C=	NP_001167618.1:p.Thr92=
NM_002316.3:c.276C=	NP_002307.2:p.Thr92=
NM_001174146.2:c.276C=	NP_001167617.1:p.Thr92=
NM_001174147.2:c.276C= MANE Select	NP_001167618.1:p.Thr92=
NM_002316.4:c.276C=	NP_002307.2:p.Thr92=