Canonical Allele Identifier: CA2488893
Gene: LMOD3 HGNC NCBI

Linked Data

dbSNP Id: rs754432774
gnomAD v2: 3-69168592-A-G
gnomAD v3: 3-69119441-A-G
gnomAD v4: 3-69119441-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69119441A>G , CM000665.2:g.69119441A>G GRCh38
NC_000003.11:g.69168592A>G , CM000665.1:g.69168592A>G GRCh37
NC_000003.10:g.69251282A>G NCBI36
NG_041828.1:g.8155T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000420581.7:c.914T>C MANE Select ENSP00000414670.3:p.Met305Thr
ENST00000420581.6:c.914T>C ENSP00000414670.2:p.Met305Thr
ENST00000475434.1:c.914T>C ENSP00000418645.1:p.Met305Thr
ENST00000489031.5:c.914T>C ENSP00000417210.1:p.Met305Thr
NM_001304418.1:c.914T>C NP_001291347.1:p.Met305Thr
NM_198271.4:c.914T>C NP_938012.2:p.Met305Thr
NM_001304418.3:c.914T>C NP_001291347.1:p.Met305Thr
NM_198271.5:c.914T>C MANE Select NP_938012.2:p.Met305Thr