Canonical Allele Identifier: CA505749522
Gene: ODAD3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.11533494G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11422826G>C , CM000681.2:g.11422826G>C GRCh38
NC_000019.9:g.11533494G>C , CM000681.1:g.11533494G>C GRCh37
NC_000019.8:g.11394494G>C NCBI36
NG_041777.1:g.17957C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356392.9:c.1152C>G MANE Select ENSP00000348757.3:p.Thr384=
ENST00000356392.8:c.1152C>G ENSP00000348757.3:p.Thr384=
ENST00000586836.5:c.579C>G ENSP00000467429.1:p.Thr193=
ENST00000591179.5:c.972C>G ENSP00000466800.1:p.Thr324=
ENST00000591345.5:c.*1071C>G ENSP00000467313.1:n.*1071C>G
NM_001302453.1:c.990C>G NP_001289382.1:p.Thr330=
NM_001302454.1:c.972C>G NP_001289383.1:p.Thr324=
NM_145045.4:c.1152C>G NP_659482.3:p.Thr384=
XM_017026241.1:c.*46C>G XP_016881730.1:n.*46C>G
NM_145045.5:c.1152C>G MANE Select NP_659482.3:p.Thr384=
NM_001302454.2:c.972C>G NP_001289383.1:p.Thr324=