Canonical Allele Identifier: CA434426546

Gene: LMOD3

Linked Data

• dbSNP Id: rs1338563122
• gnomAD v4: 3-69119407-G-A
• MyVariant Identifiers: chr3:g.69168558G>A (hg19) ; chr3:g.69119407G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69119407G>A , CM000665.2:g.69119407G>A	GRCh38
NC_000003.11:g.69168558G>A , CM000665.1:g.69168558G>A	GRCh37
NC_000003.10:g.69251248G>A	NCBI36
NG_041828.1:g.8189C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420581.7:c.948C>T MANE Select	ENSP00000414670.3:p.Asn316=
ENST00000420581.6:c.948C>T	ENSP00000414670.2:p.Asn316=
ENST00000475434.1:c.948C>T	ENSP00000418645.1:p.Asn316=
ENST00000489031.5:c.948C>T	ENSP00000417210.1:p.Asn316=
NM_001304418.1:c.948C>T	NP_001291347.1:p.Asn316=
NM_198271.4:c.948C>T	NP_938012.2:p.Asn316=
NM_001304418.3:c.948C>T	NP_001291347.1:p.Asn316=
NM_198271.5:c.948C>T MANE Select	NP_938012.2:p.Asn316=