Canonical Allele Identifier: CA353473113
Gene: LMOD3 HGNC NCBI

Linked Data

ClinVar Variation Id: 963296
ClinVar RCV Id: RCV001237303
dbSNP Id: rs2092394013
gnomAD v4: 3-69119274-C-T
MyVariant Identifiers: chr3:g.69168425C>T (hg19) chr3:g.69119274C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69119274C>T , CM000665.2:g.69119274C>T GRCh38
NC_000003.11:g.69168425C>T , CM000665.1:g.69168425C>T GRCh37
NC_000003.10:g.69251115C>T NCBI36
NG_041828.1:g.8322G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000420581.7:c.1081G>A MANE Select ENSP00000414670.3:p.Ala361Thr
ENST00000420581.6:c.1081G>A ENSP00000414670.2:p.Ala361Thr
ENST00000475434.1:c.1081G>A ENSP00000418645.1:p.Ala361Thr
ENST00000489031.5:c.1081G>A ENSP00000417210.1:p.Ala361Thr
NM_001304418.1:c.1081G>A NP_001291347.1:p.Ala361Thr
NM_198271.4:c.1081G>A NP_938012.2:p.Ala361Thr
NM_001304418.3:c.1081G>A NP_001291347.1:p.Ala361Thr
NM_198271.5:c.1081G>A MANE Select NP_938012.2:p.Ala361Thr
Search 100 bp 5'
Search 100 bp 3'