Canonical Allele Identifier: CA374913449

Gene: LMX1B

Linked Data

• gnomAD v4: 9-126693247-C-A
• MyVariant Identifiers: chr9:g.129455526C>A (hg19) ; chr9:g.126693247C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.126693247C>A , CM000671.2:g.126693247C>A	GRCh38
NC_000009.11:g.129455526C>A , CM000671.1:g.129455526C>A	GRCh37
NC_000009.10:g.128495347C>A	NCBI36
NG_017039.1:g.83805C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000355497.10:c.665C>A	ENSP00000347684.5:p.Pro222His
ENST00000373474.9:c.665C>A MANE Select	ENSP00000362573.3:p.Pro222His
ENST00000526117.6:c.665C>A	ENSP00000436930.1:p.Pro222His
ENST00000355497.9:c.665C>A	ENSP00000347684.5:p.Pro222His
ENST00000373474.8:c.665C>A	ENSP00000362573.3:p.Pro222His
ENST00000526117.5:c.665C>A	ENSP00000436930.1:p.Pro222His
ENST00000561065.1:c.596C>A	ENSP00000453580.1:p.Pro199His
NM_001174146.1:c.665C>A	NP_001167617.1:p.Pro222His
NM_001174147.1:c.665C>A	NP_001167618.1:p.Pro222His
NM_002316.3:c.665C>A	NP_002307.2:p.Pro222His
NM_001174146.2:c.665C>A	NP_001167617.1:p.Pro222His
NM_001174147.2:c.665C>A MANE Select	NP_001167618.1:p.Pro222His
NM_002316.4:c.665C>A	NP_002307.2:p.Pro222His