Canonical Allele Identifier: CA1879462904

Gene: LMX1B

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.126654038C= , CM000671.2:g.126654038C=	GRCh38
NC_000009.11:g.129416317C= , CM000671.1:g.129416317C=	GRCh37
NC_000009.10:g.128456138C=	NCBI36
NG_017039.1:g.44596C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001174147.2:c.327-36798C= MANE Select	NP_001167618.1:n.327-36798C=
ENST00000373474.9:c.327-36798C= MANE Select	ENSP00000362573.3:n.327-36798C=
NM_001174146.1:c.327-36798C=	NP_001167617.1:n.327-36798C=
NM_001174146.2:c.327-36798C=	NP_001167617.1:n.327-36798C=
NM_001174147.1:c.327-36798C=	NP_001167618.1:n.327-36798C=
NM_002316.3:c.327-36798C=	NP_002307.2:n.327-36798C=
NM_002316.4:c.327-36798C=	NP_002307.2:n.327-36798C=
ENST00000355497.10:c.327-36798C=	ENSP00000347684.5:n.327-36798C=
ENST00000355497.9:c.327-36798C=	ENSP00000347684.5:n.327-36798C=
ENST00000373474.8:c.327-36798C=	ENSP00000362573.3:n.327-36798C=
ENST00000526117.5:c.327-36798C=	ENSP00000436930.1:n.327-36798C=
ENST00000526117.6:c.327-36798C=	ENSP00000436930.1:n.327-36798C=
ENST00000561065.1:c.258-36798C=	ENSP00000453580.1:n.258-36798C=