Canonical Allele Identifier: CA467136536

Gene: LMX1B

Linked Data

• gnomAD v4: 9-126693249-C-A
• COSMIC: COSM3675233 ; COSM3675234 ; COSM3675235
• MyVariant Identifiers: chr9:g.129455528C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.126693249C>A , CM000671.2:g.126693249C>A	GRCh38
NC_000009.11:g.129455528C>A , CM000671.1:g.129455528C>A	GRCh37
NC_000009.10:g.128495349C>A	NCBI36
NG_017039.1:g.83807C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000355497.10:c.667C>A	ENSP00000347684.5:p.Arg223=
ENST00000373474.9:c.667C>A MANE Select	ENSP00000362573.3:p.Arg223=
ENST00000526117.6:c.667C>A	ENSP00000436930.1:p.Arg223=
ENST00000355497.9:c.667C>A	ENSP00000347684.5:p.Arg223=
ENST00000373474.8:c.667C>A	ENSP00000362573.3:p.Arg223=
ENST00000526117.5:c.667C>A	ENSP00000436930.1:p.Arg223=
ENST00000561065.1:c.598C>A	ENSP00000453580.1:p.Arg200=
NM_001174146.1:c.667C>A	NP_001167617.1:p.Arg223=
NM_001174147.1:c.667C>A	NP_001167618.1:p.Arg223=
NM_002316.3:c.667C>A	NP_002307.2:p.Arg223=
NM_001174146.2:c.667C>A	NP_001167617.1:p.Arg223=
NM_001174147.2:c.667C>A MANE Select	NP_001167618.1:p.Arg223=
NM_002316.4:c.667C>A	NP_002307.2:p.Arg223=