Canonical Allele Identifier: CA353474299
Gene: LMOD3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1008009
ClinVar RCV Id: RCV001305280
dbSNP Id: rs2092395759
MyVariant Identifiers: chr3:g.69168644T>G (hg19) chr3:g.69119493T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69119493T>G , CM000665.2:g.69119493T>G GRCh38
NC_000003.11:g.69168644T>G , CM000665.1:g.69168644T>G GRCh37
NC_000003.10:g.69251334T>G NCBI36
NG_041828.1:g.8103A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000420581.7:c.862A>C MANE Select ENSP00000414670.3:p.Ser288Arg
ENST00000420581.6:c.862A>C ENSP00000414670.2:p.Ser288Arg
ENST00000475434.1:c.862A>C ENSP00000418645.1:p.Ser288Arg
ENST00000489031.5:c.862A>C ENSP00000417210.1:p.Ser288Arg
NM_001304418.1:c.862A>C NP_001291347.1:p.Ser288Arg
NM_198271.4:c.862A>C NP_938012.2:p.Ser288Arg
NM_001304418.3:c.862A>C NP_001291347.1:p.Ser288Arg
NM_198271.5:c.862A>C MANE Select NP_938012.2:p.Ser288Arg
Search 100 bp 5'
Search 100 bp 3'