Canonical Allele Identifier: CA434426520
Gene: LMOD3 HGNC NCBI

Linked Data

gnomAD v4: 3-69119368-G-C
MyVariant Identifiers: chr3:g.69168519G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69119368G>C , CM000665.2:g.69119368G>C GRCh38
NC_000003.11:g.69168519G>C , CM000665.1:g.69168519G>C GRCh37
NC_000003.10:g.69251209G>C NCBI36
NG_041828.1:g.8228C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000420581.7:c.987C>G MANE Select ENSP00000414670.3:p.Ala329=
ENST00000420581.6:c.987C>G ENSP00000414670.2:p.Ala329=
ENST00000475434.1:c.987C>G ENSP00000418645.1:p.Ala329=
ENST00000489031.5:c.987C>G ENSP00000417210.1:p.Ala329=
NM_001304418.1:c.987C>G NP_001291347.1:p.Ala329=
NM_198271.4:c.987C>G NP_938012.2:p.Ala329=
NM_001304418.3:c.987C>G NP_001291347.1:p.Ala329=
NM_198271.5:c.987C>G MANE Select NP_938012.2:p.Ala329=
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