Canonical Allele Identifier: CA353473213
Gene: LMOD3 HGNC NCBI

Linked Data

dbSNP Id: rs2092394102
gnomAD v3: 3-69119291-T-C
gnomAD v4: 3-69119291-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69119291T>C , CM000665.2:g.69119291T>C GRCh38
NC_000003.11:g.69168442T>C , CM000665.1:g.69168442T>C GRCh37
NC_000003.10:g.69251132T>C NCBI36
NG_041828.1:g.8305A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000420581.7:c.1064A>G MANE Select ENSP00000414670.3:p.His355Arg
ENST00000420581.6:c.1064A>G ENSP00000414670.2:p.His355Arg
ENST00000475434.1:c.1064A>G ENSP00000418645.1:p.His355Arg
ENST00000489031.5:c.1064A>G ENSP00000417210.1:p.His355Arg
NM_001304418.1:c.1064A>G NP_001291347.1:p.His355Arg
NM_198271.4:c.1064A>G NP_938012.2:p.His355Arg
NM_001304418.3:c.1064A>G NP_001291347.1:p.His355Arg
NM_198271.5:c.1064A>G MANE Select NP_938012.2:p.His355Arg