Canonical Allele Identifier: CA2488900
Gene: LMOD3 HGNC NCBI

Linked Data

dbSNP Id: rs769630246
gnomAD v2: 3-69168629-C-T
gnomAD v4: 3-69119478-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69119478C>T , CM000665.2:g.69119478C>T GRCh38
NC_000003.11:g.69168629C>T , CM000665.1:g.69168629C>T GRCh37
NC_000003.10:g.69251319C>T NCBI36
NG_041828.1:g.8118G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000420581.7:c.877G>A MANE Select ENSP00000414670.3:p.Gly293Ser
ENST00000420581.6:c.877G>A ENSP00000414670.2:p.Gly293Ser
ENST00000475434.1:c.877G>A ENSP00000418645.1:p.Gly293Ser
ENST00000489031.5:c.877G>A ENSP00000417210.1:p.Gly293Ser
NM_001304418.1:c.877G>A NP_001291347.1:p.Gly293Ser
NM_198271.4:c.877G>A NP_938012.2:p.Gly293Ser
NM_001304418.3:c.877G>A NP_001291347.1:p.Gly293Ser
NM_198271.5:c.877G>A MANE Select NP_938012.2:p.Gly293Ser