Canonical Allele Identifier: CA467136399

Gene: LMX1B

Linked Data

• MyVariant Identifiers: chr9:g.129377816T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.126615537T>C , CM000671.2:g.126615537T>C	GRCh38
NC_000009.11:g.129377816T>C , CM000671.1:g.129377816T>C	GRCh37
NC_000009.10:g.128417637T>C	NCBI36
NG_017039.1:g.6095T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355497.10:c.294T>C	ENSP00000347684.5:p.Asp98=
ENST00000373474.9:c.294T>C MANE Select	ENSP00000362573.3:p.Asp98=
ENST00000526117.6:c.294T>C	ENSP00000436930.1:p.Asp98=
ENST00000355497.9:c.294T>C	ENSP00000347684.5:p.Asp98=
ENST00000373474.8:c.294T>C	ENSP00000362573.3:p.Asp98=
ENST00000526117.5:c.294T>C	ENSP00000436930.1:p.Asp98=
ENST00000561065.1:c.225T>C	ENSP00000453580.1:p.Asp75=
NM_001174146.1:c.294T>C	NP_001167617.1:p.Asp98=
NM_001174147.1:c.294T>C	NP_001167618.1:p.Asp98=
NM_002316.3:c.294T>C	NP_002307.2:p.Asp98=
NM_001174146.2:c.294T>C	NP_001167617.1:p.Asp98=
NM_001174147.2:c.294T>C MANE Select	NP_001167618.1:p.Asp98=
NM_002316.4:c.294T>C	NP_002307.2:p.Asp98=