Canonical Allele Identifier: CA467136533

Gene: LMX1B

Linked Data

• MyVariant Identifiers: chr9:g.129455524A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.126693245A>G , CM000671.2:g.126693245A>G	GRCh38
NC_000009.11:g.129455524A>G , CM000671.1:g.129455524A>G	GRCh37
NC_000009.10:g.128495345A>G	NCBI36
NG_017039.1:g.83803A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355497.10:c.663A>G	ENSP00000347684.5:p.Arg221=
ENST00000373474.9:c.663A>G MANE Select	ENSP00000362573.3:p.Arg221=
ENST00000526117.6:c.663A>G	ENSP00000436930.1:p.Arg221=
ENST00000355497.9:c.663A>G	ENSP00000347684.5:p.Arg221=
ENST00000373474.8:c.663A>G	ENSP00000362573.3:p.Arg221=
ENST00000526117.5:c.663A>G	ENSP00000436930.1:p.Arg221=
ENST00000561065.1:c.594A>G	ENSP00000453580.1:p.Arg198=
NM_001174146.1:c.663A>G	NP_001167617.1:p.Arg221=
NM_001174147.1:c.663A>G	NP_001167618.1:p.Arg221=
NM_002316.3:c.663A>G	NP_002307.2:p.Arg221=
NM_001174146.2:c.663A>G	NP_001167617.1:p.Arg221=
NM_001174147.2:c.663A>G MANE Select	NP_001167618.1:p.Arg221=
NM_002316.4:c.663A>G	NP_002307.2:p.Arg221=