Canonical Allele Identifier: CA305327076
Gene: ODAD3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1682764
ClinVar RCV Id: RCV002237687
dbSNP Id: rs377241671
gnomAD v2: 19-11533279-C-T
gnomAD v3: 19-11422611-C-T
gnomAD v4: 19-11422611-C-T
MyVariant Identifiers: chr19:g.11533279C>T (hg19) chr19:g.11422611C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11422611C>T , CM000681.2:g.11422611C>T GRCh38
NC_000019.9:g.11533279C>T , CM000681.1:g.11533279C>T GRCh37
NC_000019.8:g.11394279C>T NCBI36
NG_041777.1:g.18172G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356392.9:c.1294G>A MANE Select ENSP00000348757.3:p.Ala432Thr
ENST00000356392.8:c.1294G>A ENSP00000348757.3:p.Ala432Thr
ENST00000586836.5:c.721G>A ENSP00000467429.1:p.Ala241Thr
ENST00000591179.5:c.1114G>A ENSP00000466800.1:p.Ala372Thr
ENST00000591345.5:c.*1213G>A ENSP00000467313.1:n.*1213G>A
NM_001302453.1:c.1132G>A NP_001289382.1:p.Ala378Thr
NM_001302454.1:c.1114G>A NP_001289383.1:p.Ala372Thr
NM_145045.4:c.1294G>A NP_659482.3:p.Ala432Thr
NM_145045.5:c.1294G>A MANE Select NP_659482.3:p.Ala432Thr
NM_001302454.2:c.1114G>A NP_001289383.1:p.Ala372Thr
Search 100 bp 5'
Search 100 bp 3'