Canonical Allele Identifier: CA632116944

Gene: ODAD3

Linked Data

• dbSNP Id: rs1479501587
• gnomAD v2: 19-11533317-C-T
• gnomAD v3: 19-11422649-C-T
• gnomAD v4: 19-11422649-C-T
• MyVariant Identifiers: chr19:g.11533317C>T (hg19) ; chr19:g.11422649C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11422649C>T , CM000681.2:g.11422649C>T	GRCh38
NC_000019.9:g.11533317C>T , CM000681.1:g.11533317C>T	GRCh37
NC_000019.8:g.11394317C>T	NCBI36
NG_041777.1:g.18134G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356392.9:c.1278-22G>A MANE Select	ENSP00000348757.3:n.1278-22G>A
ENST00000356392.8:c.1278-22G>A	ENSP00000348757.3:n.1278-22G>A
ENST00000586836.5:c.705-22G>A	ENSP00000467429.1:n.705-22G>A
ENST00000591179.5:c.1098-22G>A	ENSP00000466800.1:n.1098-22G>A
ENST00000591345.5:c.*1197-22G>A	ENSP00000467313.1:n.*1197-22G>A
NM_001302453.1:c.1116-22G>A	NP_001289382.1:n.1116-22G>A
NM_001302454.1:c.1098-22G>A	NP_001289383.1:n.1098-22G>A
NM_145045.4:c.1278-22G>A	NP_659482.3:n.1278-22G>A
NM_145045.5:c.1278-22G>A MANE Select	NP_659482.3:n.1278-22G>A
NM_001302454.2:c.1098-22G>A	NP_001289383.1:n.1098-22G>A