Canonical Allele Identifier: CA353473706
Gene: LMOD3 HGNC NCBI

Linked Data

dbSNP Id: rs2092395013

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69119390A>G , CM000665.2:g.69119390A>G GRCh38
NC_000003.11:g.69168541A>G , CM000665.1:g.69168541A>G GRCh37
NC_000003.10:g.69251231A>G NCBI36
NG_041828.1:g.8206T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000420581.7:c.965T>C MANE Select ENSP00000414670.3:p.Ile322Thr
ENST00000420581.6:c.965T>C ENSP00000414670.2:p.Ile322Thr
ENST00000475434.1:c.965T>C ENSP00000418645.1:p.Ile322Thr
ENST00000489031.5:c.965T>C ENSP00000417210.1:p.Ile322Thr
NM_001304418.1:c.965T>C NP_001291347.1:p.Ile322Thr
NM_198271.4:c.965T>C NP_938012.2:p.Ile322Thr
NM_001304418.3:c.965T>C NP_001291347.1:p.Ile322Thr
NM_198271.5:c.965T>C MANE Select NP_938012.2:p.Ile322Thr