Canonical Allele Identifier: CA860119111

Gene: LMX1B

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.126698635A>T , CM000671.2:g.126698635A>T	GRCh38
NC_000009.11:g.129460914A>T , CM000671.1:g.129460914A>T	GRCh37
NC_000009.10:g.128500735A>T	NCBI36
NG_017039.1:g.89193A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355497.10:c.*2184A>T	ENSP00000347684.5:n.*2184A>T
ENST00000373474.9:c.*2184A>T MANE Select	ENSP00000362573.3:n.*2184A>T
ENST00000526117.6:c.*2184A>T	ENSP00000436930.1:n.*2184A>T
ENST00000355497.9:c.*2184A>T	ENSP00000347684.5:n.*2184A>T
ENST00000373474.8:c.*2184A>T	ENSP00000362573.3:n.*2184A>T
NM_001174146.1:c.*2184A>T	NP_001167617.1:n.*2184A>T
NM_001174147.1:c.*2184A>T	NP_001167618.1:n.*2184A>T
NM_002316.3:c.*2184A>T	NP_002307.2:n.*2184A>T
NM_001174146.2:c.*2184A>T	NP_001167617.1:n.*2184A>T
NM_001174147.2:c.*2184A>T MANE Select	NP_001167618.1:n.*2184A>T
NM_002316.4:c.*2184A>T	NP_002307.2:n.*2184A>T