Canonical Allele Identifier: CA1879436147
Gene: LMX1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.126615390C= , CM000671.2:g.126615390C= GRCh38
NC_000009.11:g.129377669C= , CM000671.1:g.129377669C= GRCh37
NC_000009.10:g.128417490C= NCBI36
NG_017039.1:g.5948C=

Transcript Alleles

HGVS Amino-acid change
ENST00000355497.10:c.147C= ENSP00000347684.5:p.Asp49=
ENST00000373474.9:c.147C= MANE Select ENSP00000362573.3:p.Asp49=
ENST00000526117.6:c.147C= ENSP00000436930.1:p.Asp49=
ENST00000355497.9:c.147C= ENSP00000347684.5:p.Asp49=
ENST00000373474.8:c.147C= ENSP00000362573.3:p.Asp49=
ENST00000526117.5:c.147C= ENSP00000436930.1:p.Asp49=
ENST00000561065.1:c.78C= ENSP00000453580.1:p.Asp26=
NM_001174146.1:c.147C= NP_001167617.1:p.Asp49=
NM_001174147.1:c.147C= NP_001167618.1:p.Asp49=
NM_002316.3:c.147C= NP_002307.2:p.Asp49=
NM_001174146.2:c.147C= NP_001167617.1:p.Asp49=
NM_001174147.2:c.147C= MANE Select NP_001167618.1:p.Asp49=
NM_002316.4:c.147C= NP_002307.2:p.Asp49=