Canonical Allele Identifier: CA404122936

Gene: ODAD3

Linked Data

• ClinVar Variation Id: 662085
• ClinVar RCV Id: RCV000819651
• dbSNP Id: rs375587857
• gnomAD v2: 19-11537008-G-C
• gnomAD v3: 19-11426188-G-C
• gnomAD v4: 19-11426188-G-C
• MyVariant Identifiers: chr19:g.11537008G>C (hg19) ; chr19:g.11426188G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11426188G>C , CM000681.2:g.11426188G>C	GRCh38
NC_000019.9:g.11537008G>C , CM000681.1:g.11537008G>C	GRCh37
NC_000019.8:g.11398008G>C	NCBI36
NG_041777.1:g.14595C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000356392.9:c.919C>G MANE Select	ENSP00000348757.3:p.Arg307Gly
ENST00000356392.8:c.919C>G	ENSP00000348757.3:p.Arg307Gly
ENST00000586836.5:c.346C>G	ENSP00000467429.1:p.Arg116Gly
ENST00000591179.5:c.739C>G	ENSP00000466800.1:p.Arg247Gly
ENST00000591345.5:c.*838C>G	ENSP00000467313.1:n.*838C>G
NM_001302453.1:c.757C>G	NP_001289382.1:p.Arg253Gly
NM_001302454.1:c.739C>G	NP_001289383.1:p.Arg247Gly
NM_145045.4:c.919C>G	NP_659482.3:p.Arg307Gly
XM_017026241.1:c.904+15C>G	XP_016881730.1:n.904+15C>G
NM_145045.5:c.919C>G MANE Select	NP_659482.3:p.Arg307Gly
NM_001302454.2:c.739C>G	NP_001289383.1:p.Arg247Gly