Canonical Allele Identifier: CA9212213

Gene: ODAD3

Linked Data

• dbSNP Id: rs61739937
• ExAC: 19:11537006 G / C
• gnomAD v2: 19-11537006-G-C
• gnomAD v4: 19-11426186-G-C
• MyVariant Identifiers: chr19:g.11537006G>C (hg19) ; chr19:g.11426186G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11426186G>C , CM000681.2:g.11426186G>C	GRCh38
NC_000019.9:g.11537006G>C , CM000681.1:g.11537006G>C	GRCh37
NC_000019.8:g.11398006G>C	NCBI36
NG_041777.1:g.14597C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000356392.9:c.921C>G MANE Select	ENSP00000348757.3:p.Arg307=
ENST00000356392.8:c.921C>G	ENSP00000348757.3:p.Arg307=
ENST00000586836.5:c.348C>G	ENSP00000467429.1:p.Arg116=
ENST00000591179.5:c.741C>G	ENSP00000466800.1:p.Arg247=
ENST00000591345.5:c.*840C>G	ENSP00000467313.1:n.*840C>G
NM_001302453.1:c.759C>G	NP_001289382.1:p.Arg253=
NM_001302454.1:c.741C>G	NP_001289383.1:p.Arg247=
NM_145045.4:c.921C>G	NP_659482.3:p.Arg307=
XM_017026241.1:c.904+17C>G	XP_016881730.1:n.904+17C>G
NM_145045.5:c.921C>G MANE Select	NP_659482.3:p.Arg307=
NM_001302454.2:c.741C>G	NP_001289383.1:p.Arg247=