Canonical Allele Identifier: CA404119858

Gene: ODAD3

Linked Data

• dbSNP Id: rs756157252
• gnomAD v2: 19-11533264-G-A
• gnomAD v3: 19-11422596-G-A
• gnomAD v4: 19-11422596-G-A
• MyVariant Identifiers: chr19:g.11533264G>A (hg19) ; chr19:g.11422596G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11422596G>A , CM000681.2:g.11422596G>A	GRCh38
NC_000019.9:g.11533264G>A , CM000681.1:g.11533264G>A	GRCh37
NC_000019.8:g.11394264G>A	NCBI36
NG_041777.1:g.18187C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356392.9:c.1309C>T MANE Select	ENSP00000348757.3:p.Arg437Cys
ENST00000356392.8:c.1309C>T	ENSP00000348757.3:p.Arg437Cys
ENST00000586836.5:c.736C>T	ENSP00000467429.1:p.Arg246Cys
ENST00000591179.5:c.1129C>T	ENSP00000466800.1:p.Arg377Cys
ENST00000591345.5:c.*1228C>T	ENSP00000467313.1:n.*1228C>T
NM_001302453.1:c.1147C>T	NP_001289382.1:p.Arg383Cys
NM_001302454.1:c.1129C>T	NP_001289383.1:p.Arg377Cys
NM_145045.4:c.1309C>T	NP_659482.3:p.Arg437Cys
NM_145045.5:c.1309C>T MANE Select	NP_659482.3:p.Arg437Cys
NM_001302454.2:c.1129C>T	NP_001289383.1:p.Arg377Cys