Canonical Allele Identifier: CA9212194

Gene: ODAD3

Linked Data

• dbSNP Id: rs756658850
• ExAC: 19:11536935 C / T
• gnomAD v2: 19-11536935-C-T
• gnomAD v4: 19-11426115-C-T
• MyVariant Identifiers: chr19:g.11536935C>T (hg19) ; chr19:g.11426115C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11426115C>T , CM000681.2:g.11426115C>T	GRCh38
NC_000019.9:g.11536935C>T , CM000681.1:g.11536935C>T	GRCh37
NC_000019.8:g.11397935C>T	NCBI36
NG_041777.1:g.14668G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356392.9:c.963+29G>A MANE Select	ENSP00000348757.3:n.963+29G>A
ENST00000356392.8:c.963+29G>A	ENSP00000348757.3:n.963+29G>A
ENST00000586836.5:c.390+29G>A	ENSP00000467429.1:n.390+29G>A
ENST00000591179.5:c.783+29G>A	ENSP00000466800.1:n.783+29G>A
ENST00000591345.5:c.*882+29G>A	ENSP00000467313.1:n.*882+29G>A
NM_001302453.1:c.801+29G>A	NP_001289382.1:n.801+29G>A
NM_001302454.1:c.783+29G>A	NP_001289383.1:n.783+29G>A
NM_145045.4:c.963+29G>A	NP_659482.3:n.963+29G>A
XM_017026241.1:c.904+88G>A	XP_016881730.1:n.904+88G>A
NM_145045.5:c.963+29G>A MANE Select	NP_659482.3:n.963+29G>A
NM_001302454.2:c.783+29G>A	NP_001289383.1:n.783+29G>A