Canonical Allele Identifier: CA632116955

Gene: ODAD3

Linked Data

• dbSNP Id: rs1295384165
• gnomAD v2: 19-11536919-T-C
• gnomAD v3: 19-11426099-T-C
• gnomAD v4: 19-11426099-T-C
• MyVariant Identifiers: chr19:g.11536919T>C (hg19) ; chr19:g.11426099T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11426099T>C , CM000681.2:g.11426099T>C	GRCh38
NC_000019.9:g.11536919T>C , CM000681.1:g.11536919T>C	GRCh37
NC_000019.8:g.11397919T>C	NCBI36
NG_041777.1:g.14684A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356392.9:c.963+45A>G MANE Select	ENSP00000348757.3:n.963+45A>G
ENST00000356392.8:c.963+45A>G	ENSP00000348757.3:n.963+45A>G
ENST00000586836.5:c.390+45A>G	ENSP00000467429.1:n.390+45A>G
ENST00000591179.5:c.783+45A>G	ENSP00000466800.1:n.783+45A>G
ENST00000591345.5:c.*882+45A>G	ENSP00000467313.1:n.*882+45A>G
NM_001302453.1:c.801+45A>G	NP_001289382.1:n.801+45A>G
NM_001302454.1:c.783+45A>G	NP_001289383.1:n.783+45A>G
NM_145045.4:c.963+45A>G	NP_659482.3:n.963+45A>G
XM_017026241.1:c.904+104A>G	XP_016881730.1:n.904+104A>G
NM_145045.5:c.963+45A>G MANE Select	NP_659482.3:n.963+45A>G
NM_001302454.2:c.783+45A>G	NP_001289383.1:n.783+45A>G