Canonical Allele Identifier: CA353473660
Gene: LMOD3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1055832
ClinVar RCV Id: RCV001364566
dbSNP Id: rs2107526347

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69119379C>G , CM000665.2:g.69119379C>G GRCh38
NC_000003.11:g.69168530C>G , CM000665.1:g.69168530C>G GRCh37
NC_000003.10:g.69251220C>G NCBI36
NG_041828.1:g.8217G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000420581.7:c.976G>C MANE Select ENSP00000414670.3:p.Gly326Arg
ENST00000420581.6:c.976G>C ENSP00000414670.2:p.Gly326Arg
ENST00000475434.1:c.976G>C ENSP00000418645.1:p.Gly326Arg
ENST00000489031.5:c.976G>C ENSP00000417210.1:p.Gly326Arg
NM_001304418.1:c.976G>C NP_001291347.1:p.Gly326Arg
NM_198271.4:c.976G>C NP_938012.2:p.Gly326Arg
NM_001304418.3:c.976G>C NP_001291347.1:p.Gly326Arg
NM_198271.5:c.976G>C MANE Select NP_938012.2:p.Gly326Arg