Canonical Allele Identifier: CA783271493

Gene: ODAD3

Linked Data

• dbSNP Id: rs1276133032
• MyVariant Identifiers: chr19:g.11533684G>T (hg19) ; chr19:g.11423016G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11423016G>T , CM000681.2:g.11423016G>T	GRCh38
NC_000019.9:g.11533684G>T , CM000681.1:g.11533684G>T	GRCh37
NC_000019.8:g.11394684G>T	NCBI36
NG_041777.1:g.17767C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356392.9:c.1117-155C>A MANE Select	ENSP00000348757.3:n.1117-155C>A
ENST00000356392.8:c.1117-155C>A	ENSP00000348757.3:n.1117-155C>A
ENST00000586836.5:c.544-155C>A	ENSP00000467429.1:n.544-155C>A
ENST00000591179.5:c.937-155C>A	ENSP00000466800.1:n.937-155C>A
ENST00000591345.5:c.*1036-155C>A	ENSP00000467313.1:n.*1036-155C>A
NM_001302453.1:c.955-155C>A	NP_001289382.1:n.955-155C>A
NM_001302454.1:c.937-155C>A	NP_001289383.1:n.937-155C>A
NM_145045.4:c.1117-155C>A	NP_659482.3:n.1117-155C>A
XM_017026241.1:c.*11-155C>A	XP_016881730.1:n.*11-155C>A
NM_145045.5:c.1117-155C>A MANE Select	NP_659482.3:n.1117-155C>A
NM_001302454.2:c.937-155C>A	NP_001289383.1:n.937-155C>A