Canonical Allele Identifier: CA434426676

Gene: LMOD3

Linked Data

• dbSNP Id: rs1312341772
• gnomAD v4: 3-69119497-T-C
• MyVariant Identifiers: chr3:g.69168648T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69119497T>C , CM000665.2:g.69119497T>C	GRCh38
NC_000003.11:g.69168648T>C , CM000665.1:g.69168648T>C	GRCh37
NC_000003.10:g.69251338T>C	NCBI36
NG_041828.1:g.8099A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420581.7:c.858A>G MANE Select	ENSP00000414670.3:p.Thr286=
ENST00000420581.6:c.858A>G	ENSP00000414670.2:p.Thr286=
ENST00000475434.1:c.858A>G	ENSP00000418645.1:p.Thr286=
ENST00000489031.5:c.858A>G	ENSP00000417210.1:p.Thr286=
NM_001304418.1:c.858A>G	NP_001291347.1:p.Thr286=
NM_198271.4:c.858A>G	NP_938012.2:p.Thr286=
NM_001304418.3:c.858A>G	NP_001291347.1:p.Thr286=
NM_198271.5:c.858A>G MANE Select	NP_938012.2:p.Thr286=