Canonical Allele Identifier: CA353473859

Gene: LMOD3

Linked Data

• dbSNP Id: rs1319708395
• gnomAD v2: 3-69168566-T-C
• gnomAD v4: 3-69119415-T-C
• MyVariant Identifiers: chr3:g.69168566T>C (hg19) ; chr3:g.69119415T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69119415T>C , CM000665.2:g.69119415T>C	GRCh38
NC_000003.11:g.69168566T>C , CM000665.1:g.69168566T>C	GRCh37
NC_000003.10:g.69251256T>C	NCBI36
NG_041828.1:g.8181A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420581.7:c.940A>G MANE Select	ENSP00000414670.3:p.Thr314Ala
ENST00000420581.6:c.940A>G	ENSP00000414670.2:p.Thr314Ala
ENST00000475434.1:c.940A>G	ENSP00000418645.1:p.Thr314Ala
ENST00000489031.5:c.940A>G	ENSP00000417210.1:p.Thr314Ala
NM_001304418.1:c.940A>G	NP_001291347.1:p.Thr314Ala
NM_198271.4:c.940A>G	NP_938012.2:p.Thr314Ala
NM_001304418.3:c.940A>G	NP_001291347.1:p.Thr314Ala
NM_198271.5:c.940A>G MANE Select	NP_938012.2:p.Thr314Ala