Canonical Allele Identifier: CA353473422

Gene: LMOD3

Linked Data

• dbSNP Id: rs2092394425
• gnomAD v3: 3-69119333-G-A
• gnomAD v4: 3-69119333-G-A
• MyVariant Identifiers: chr3:g.69168484G>A (hg19) ; chr3:g.69119333G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69119333G>A , CM000665.2:g.69119333G>A	GRCh38
NC_000003.11:g.69168484G>A , CM000665.1:g.69168484G>A	GRCh37
NC_000003.10:g.69251174G>A	NCBI36
NG_041828.1:g.8263C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420581.7:c.1022C>T MANE Select	ENSP00000414670.3:p.Thr341Ile
ENST00000420581.6:c.1022C>T	ENSP00000414670.2:p.Thr341Ile
ENST00000475434.1:c.1022C>T	ENSP00000418645.1:p.Thr341Ile
ENST00000489031.5:c.1022C>T	ENSP00000417210.1:p.Thr341Ile
NM_001304418.1:c.1022C>T	NP_001291347.1:p.Thr341Ile
NM_198271.4:c.1022C>T	NP_938012.2:p.Thr341Ile
NM_001304418.3:c.1022C>T	NP_001291347.1:p.Thr341Ile
NM_198271.5:c.1022C>T MANE Select	NP_938012.2:p.Thr341Ile