Canonical Allele Identifier: CA505749535
Gene: ODAD3 HGNC NCBI

Linked Data

dbSNP Id: rs1969173007
MyVariant Identifiers: chr19:g.11533506G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11422838G>C , CM000681.2:g.11422838G>C GRCh38
NC_000019.9:g.11533506G>C , CM000681.1:g.11533506G>C GRCh37
NC_000019.8:g.11394506G>C NCBI36
NG_041777.1:g.17945C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356392.9:c.1140C>G MANE Select ENSP00000348757.3:p.Ala380=
ENST00000356392.8:c.1140C>G ENSP00000348757.3:p.Ala380=
ENST00000586836.5:c.567C>G ENSP00000467429.1:p.Ala189=
ENST00000591179.5:c.960C>G ENSP00000466800.1:p.Ala320=
ENST00000591345.5:c.*1059C>G ENSP00000467313.1:n.*1059C>G
NM_001302453.1:c.978C>G NP_001289382.1:p.Ala326=
NM_001302454.1:c.960C>G NP_001289383.1:p.Ala320=
NM_145045.4:c.1140C>G NP_659482.3:p.Ala380=
XM_017026241.1:c.*34C>G XP_016881730.1:n.*34C>G
NM_145045.5:c.1140C>G MANE Select NP_659482.3:p.Ala380=
NM_001302454.2:c.960C>G NP_001289383.1:p.Ala320=