Canonical Allele Identifier: CA353473692
Gene: LMOD3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.69168538G>C (hg19) chr3:g.69119387G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69119387G>C , CM000665.2:g.69119387G>C GRCh38
NC_000003.11:g.69168538G>C , CM000665.1:g.69168538G>C GRCh37
NC_000003.10:g.69251228G>C NCBI36
NG_041828.1:g.8209C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000420581.7:c.968C>G MANE Select ENSP00000414670.3:p.Thr323Arg
ENST00000420581.6:c.968C>G ENSP00000414670.2:p.Thr323Arg
ENST00000475434.1:c.968C>G ENSP00000418645.1:p.Thr323Arg
ENST00000489031.5:c.968C>G ENSP00000417210.1:p.Thr323Arg
NM_001304418.1:c.968C>G NP_001291347.1:p.Thr323Arg
NM_198271.4:c.968C>G NP_938012.2:p.Thr323Arg
NM_001304418.3:c.968C>G NP_001291347.1:p.Thr323Arg
NM_198271.5:c.968C>G MANE Select NP_938012.2:p.Thr323Arg
Search 100 bp 5'
Search 100 bp 3'