Canonical Allele Identifier: CA31864873
Gene: LMX1A HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11809911

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165319120T>C , CM000663.2:g.165319120T>C GRCh38
NC_000001.10:g.165288357T>C , CM000663.1:g.165288357T>C GRCh37
NC_000001.9:g.163554981T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001174069.1:c.263+33956A>G VV NP_001167540.1:p.=
NM_177398.3:c.263+33956A>G VV NP_796372.1:p.=
XM_011509540.1:c.263+33956A>G XP_011507842.1:p.=
XM_011509540.2:c.263+33956A>G XP_011507842.1:p.=
NM_177398.4:c.263+33956A>G VV MANE Preferred NP_796372.1:p.=
ENST00000294816.6:c.263+33956A>G ENSP00000294816.2:p.=
ENST00000342310.7:c.263+33956A>G ENSP00000340226.3:p.=
ENST00000367893.4:c.263+33956A>G ENSP00000356868.4:p.=