Canonical Allele Identifier: CA353474174

Gene: LMOD3

Linked Data

• dbSNP Id: rs1170085948
• gnomAD v2: 3-69168622-T-A
• gnomAD v4: 3-69119471-T-A
• MyVariant Identifiers: chr3:g.69168622T>A (hg19) ; chr3:g.69119471T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69119471T>A , CM000665.2:g.69119471T>A	GRCh38
NC_000003.11:g.69168622T>A , CM000665.1:g.69168622T>A	GRCh37
NC_000003.10:g.69251312T>A	NCBI36
NG_041828.1:g.8125A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420581.7:c.884A>T MANE Select	ENSP00000414670.3:p.Asp295Val
ENST00000420581.6:c.884A>T	ENSP00000414670.2:p.Asp295Val
ENST00000475434.1:c.884A>T	ENSP00000418645.1:p.Asp295Val
ENST00000489031.5:c.884A>T	ENSP00000417210.1:p.Asp295Val
NM_001304418.1:c.884A>T	NP_001291347.1:p.Asp295Val
NM_198271.4:c.884A>T	NP_938012.2:p.Asp295Val
NM_001304418.3:c.884A>T	NP_001291347.1:p.Asp295Val
NM_198271.5:c.884A>T MANE Select	NP_938012.2:p.Asp295Val