Canonical Allele Identifier: CA1879436059
Gene: LMX1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.126615253C= , CM000671.2:g.126615253C= GRCh38
NC_000009.11:g.129377532C= , CM000671.1:g.129377532C= GRCh37
NC_000009.10:g.128417353C= NCBI36
NG_017039.1:g.5811C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355497.10:c.140-130C= ENSP00000347684.5:n.140-130C=
ENST00000373474.9:c.140-130C= MANE Select ENSP00000362573.3:n.140-130C=
ENST00000526117.6:c.140-130C= ENSP00000436930.1:n.140-130C=
ENST00000355497.9:c.140-130C= ENSP00000347684.5:n.140-130C=
ENST00000373474.8:c.140-130C= ENSP00000362573.3:n.140-130C=
ENST00000526117.5:c.140-130C= ENSP00000436930.1:n.140-130C=
ENST00000561065.1:c.71-130C= ENSP00000453580.1:n.71-130C=
NM_001174146.1:c.140-130C= NP_001167617.1:n.140-130C=
NM_001174147.1:c.140-130C= NP_001167618.1:n.140-130C=
NM_002316.3:c.140-130C= NP_002307.2:n.140-130C=
NM_001174146.2:c.140-130C= NP_001167617.1:n.140-130C=
NM_001174147.2:c.140-130C= MANE Select NP_001167618.1:n.140-130C=
NM_002316.4:c.140-130C= NP_002307.2:n.140-130C=