Canonical Allele Identifier: CA353473055
Gene: LMOD3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.69168412T>C (hg19) chr3:g.69119261T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69119261T>C , CM000665.2:g.69119261T>C GRCh38
NC_000003.11:g.69168412T>C , CM000665.1:g.69168412T>C GRCh37
NC_000003.10:g.69251102T>C NCBI36
NG_041828.1:g.8335A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000420581.7:c.1094A>G MANE Select ENSP00000414670.3:p.Lys365Arg
ENST00000420581.6:c.1094A>G ENSP00000414670.2:p.Lys365Arg
ENST00000475434.1:c.1094A>G ENSP00000418645.1:p.Lys365Arg
ENST00000489031.5:c.1094A>G ENSP00000417210.1:p.Lys365Arg
NM_001304418.1:c.1094A>G NP_001291347.1:p.Lys365Arg
NM_198271.4:c.1094A>G NP_938012.2:p.Lys365Arg
NM_001304418.3:c.1094A>G NP_001291347.1:p.Lys365Arg
NM_198271.5:c.1094A>G MANE Select NP_938012.2:p.Lys365Arg
Search 100 bp 5'
Search 100 bp 3'