Canonical Allele Identifier: CA2488907
Gene: LMOD3 HGNC NCBI

Linked Data

dbSNP Id: rs773048057
ExAC: 3:69168657 G / T
gnomAD v2: 3-69168657-G-T
gnomAD v4: 3-69119506-G-T
MyVariant Identifiers: chr3:g.69168657G>T (hg19) chr3:g.69119506G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69119506G>T , CM000665.2:g.69119506G>T GRCh38
NC_000003.11:g.69168657G>T , CM000665.1:g.69168657G>T GRCh37
NC_000003.10:g.69251347G>T NCBI36
NG_041828.1:g.8090C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000420581.7:c.849C>A MANE Select ENSP00000414670.3:p.His283Gln
ENST00000420581.6:c.849C>A ENSP00000414670.2:p.His283Gln
ENST00000475434.1:c.849C>A ENSP00000418645.1:p.His283Gln
ENST00000489031.5:c.849C>A ENSP00000417210.1:p.His283Gln
NM_001304418.1:c.849C>A NP_001291347.1:p.His283Gln
NM_198271.4:c.849C>A NP_938012.2:p.His283Gln
NM_001304418.3:c.849C>A NP_001291347.1:p.His283Gln
NM_198271.5:c.849C>A MANE Select NP_938012.2:p.His283Gln
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