Canonical Allele Identifier: CA305327400

Gene: ODAD3

Linked Data

• dbSNP Id: rs975377808
• gnomAD v3: 19-11422949-A-G
• gnomAD v4: 19-11422949-A-G
• MyVariant Identifiers: chr19:g.11533617A>G (hg19) ; chr19:g.11422949A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11422949A>G , CM000681.2:g.11422949A>G	GRCh38
NC_000019.9:g.11533617A>G , CM000681.1:g.11533617A>G	GRCh37
NC_000019.8:g.11394617A>G	NCBI36
NG_041777.1:g.17834T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356392.9:c.1117-88T>C MANE Select	ENSP00000348757.3:n.1117-88T>C
ENST00000356392.8:c.1117-88T>C	ENSP00000348757.3:n.1117-88T>C
ENST00000586836.5:c.544-88T>C	ENSP00000467429.1:n.544-88T>C
ENST00000591179.5:c.937-88T>C	ENSP00000466800.1:n.937-88T>C
ENST00000591345.5:c.*1036-88T>C	ENSP00000467313.1:n.*1036-88T>C
NM_001302453.1:c.955-88T>C	NP_001289382.1:n.955-88T>C
NM_001302454.1:c.937-88T>C	NP_001289383.1:n.937-88T>C
NM_145045.4:c.1117-88T>C	NP_659482.3:n.1117-88T>C
XM_017026241.1:c.*11-88T>C	XP_016881730.1:n.*11-88T>C
NM_145045.5:c.1117-88T>C MANE Select	NP_659482.3:n.1117-88T>C
NM_001302454.2:c.937-88T>C	NP_001289383.1:n.937-88T>C