Canonical Allele Identifier: CA353474256
Gene: LMOD3 HGNC NCBI

Linked Data

dbSNP Id: rs1342213531

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69119486G>C , CM000665.2:g.69119486G>C GRCh38
NC_000003.11:g.69168637G>C , CM000665.1:g.69168637G>C GRCh37
NC_000003.10:g.69251327G>C NCBI36
NG_041828.1:g.8110C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000420581.7:c.869C>G MANE Select ENSP00000414670.3:p.Ala290Gly
ENST00000420581.6:c.869C>G ENSP00000414670.2:p.Ala290Gly
ENST00000475434.1:c.869C>G ENSP00000418645.1:p.Ala290Gly
ENST00000489031.5:c.869C>G ENSP00000417210.1:p.Ala290Gly
NM_001304418.1:c.869C>G NP_001291347.1:p.Ala290Gly
NM_198271.4:c.869C>G NP_938012.2:p.Ala290Gly
NM_001304418.3:c.869C>G NP_001291347.1:p.Ala290Gly
NM_198271.5:c.869C>G MANE Select NP_938012.2:p.Ala290Gly