Canonical Allele Identifier: CA2488878
Gene: LMOD3 HGNC NCBI

Linked Data

dbSNP Id: rs776501883
ExAC: 3:69168514 A / G
gnomAD v2: 3-69168514-A-G
gnomAD v4: 3-69119363-A-G
COSMIC: COSM3597249 COSM3597250
MyVariant Identifiers: chr3:g.69168514A>G (hg19) chr3:g.69119363A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69119363A>G , CM000665.2:g.69119363A>G GRCh38
NC_000003.11:g.69168514A>G , CM000665.1:g.69168514A>G GRCh37
NC_000003.10:g.69251204A>G NCBI36
NG_041828.1:g.8233T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000420581.7:c.992T>C MANE Select ENSP00000414670.3:p.Met331Thr
ENST00000420581.6:c.992T>C ENSP00000414670.2:p.Met331Thr
ENST00000475434.1:c.992T>C ENSP00000418645.1:p.Met331Thr
ENST00000489031.5:c.992T>C ENSP00000417210.1:p.Met331Thr
NM_001304418.1:c.992T>C NP_001291347.1:p.Met331Thr
NM_198271.4:c.992T>C NP_938012.2:p.Met331Thr
NM_001304418.3:c.992T>C NP_001291347.1:p.Met331Thr
NM_198271.5:c.992T>C MANE Select NP_938012.2:p.Met331Thr
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