Canonical Allele Identifier: CA505749571
Gene: ODAD3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.11537021A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11426201A>G , CM000681.2:g.11426201A>G GRCh38
NC_000019.9:g.11537021A>G , CM000681.1:g.11537021A>G GRCh37
NC_000019.8:g.11398021A>G NCBI36
NG_041777.1:g.14582T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356392.9:c.906T>C MANE Select ENSP00000348757.3:p.Ser302=
ENST00000356392.8:c.906T>C ENSP00000348757.3:p.Ser302=
ENST00000586836.5:c.333T>C ENSP00000467429.1:p.Ser111=
ENST00000591179.5:c.726T>C ENSP00000466800.1:p.Ser242=
ENST00000591345.5:c.*825T>C ENSP00000467313.1:n.*825T>C
NM_001302453.1:c.744T>C NP_001289382.1:p.Ser248=
NM_001302454.1:c.726T>C NP_001289383.1:p.Ser242=
NM_145045.4:c.906T>C NP_659482.3:p.Ser302=
XM_017026241.1:c.904+2T>C XP_016881730.1:n.904+2T>C
NM_145045.5:c.906T>C MANE Select NP_659482.3:p.Ser302=
NM_001302454.2:c.726T>C NP_001289383.1:p.Ser242=