Canonical Allele Identifier: CA199816051

Gene: LMX1B

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.126695762T>A , CM000671.2:g.126695762T>A	GRCh38
NC_000009.11:g.129458041T>A , CM000671.1:g.129458041T>A	GRCh37
NC_000009.10:g.128497862T>A	NCBI36
NG_017039.1:g.86320T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001174147.2:c.887-77T>A MANE Select	NP_001167618.1:n.887-77T>A
ENST00000373474.9:c.887-77T>A MANE Select	ENSP00000362573.3:n.887-77T>A
NM_001174146.1:c.920-77T>A	NP_001167617.1:n.920-77T>A
NM_001174146.2:c.920-77T>A	NP_001167617.1:n.920-77T>A
NM_001174147.1:c.887-77T>A	NP_001167618.1:n.887-77T>A
NM_002316.3:c.887-77T>A	NP_002307.2:n.887-77T>A
NM_002316.4:c.887-77T>A	NP_002307.2:n.887-77T>A
ENST00000355497.10:c.920-77T>A	ENSP00000347684.5:n.920-77T>A
ENST00000355497.9:c.920-77T>A	ENSP00000347684.5:n.920-77T>A
ENST00000373474.8:c.887-77T>A	ENSP00000362573.3:n.887-77T>A
ENST00000526117.5:c.887-77T>A	ENSP00000436930.1:n.887-77T>A
ENST00000526117.6:c.887-77T>A	ENSP00000436930.1:n.887-77T>A
ENST00000561065.1:c.851-77T>A	ENSP00000453580.1:n.851-77T>A