Canonical Allele Identifier: CA505749470
Gene: ODAD3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1911613
ClinVar RCV Id: RCV002578628
dbSNP Id: rs940789605
gnomAD v2: 19-11533407-C-G
gnomAD v3: 19-11422739-C-G
gnomAD v4: 19-11422739-C-G
MyVariant Identifiers: chr19:g.11533407C>G (hg19) chr19:g.11422739C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11422739C>G , CM000681.2:g.11422739C>G GRCh38
NC_000019.9:g.11533407C>G , CM000681.1:g.11533407C>G GRCh37
NC_000019.8:g.11394407C>G NCBI36
NG_041777.1:g.18044G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356392.9:c.1239G>C MANE Select ENSP00000348757.3:p.Leu413=
ENST00000356392.8:c.1239G>C ENSP00000348757.3:p.Leu413=
ENST00000586836.5:c.666G>C ENSP00000467429.1:p.Leu222=
ENST00000591179.5:c.1059G>C ENSP00000466800.1:p.Leu353=
ENST00000591345.5:c.*1158G>C ENSP00000467313.1:n.*1158G>C
NM_001302453.1:c.1077G>C NP_001289382.1:p.Leu359=
NM_001302454.1:c.1059G>C NP_001289383.1:p.Leu353=
NM_145045.4:c.1239G>C NP_659482.3:p.Leu413=
NM_145045.5:c.1239G>C MANE Select NP_659482.3:p.Leu413=
NM_001302454.2:c.1059G>C NP_001289383.1:p.Leu353=
Search 100 bp 5'
Search 100 bp 3'