Canonical Allele Identifier: CA404122778

Gene: ODAD3

Linked Data

• dbSNP Id: rs1165764043
• gnomAD v2: 19-11536974-A-G
• gnomAD v4: 19-11426154-A-G
• MyVariant Identifiers: chr19:g.11536974A>G (hg19) ; chr19:g.11426154A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11426154A>G , CM000681.2:g.11426154A>G	GRCh38
NC_000019.9:g.11536974A>G , CM000681.1:g.11536974A>G	GRCh37
NC_000019.8:g.11397974A>G	NCBI36
NG_041777.1:g.14629T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356392.9:c.953T>C MANE Select	ENSP00000348757.3:p.Met318Thr
ENST00000356392.8:c.953T>C	ENSP00000348757.3:p.Met318Thr
ENST00000586836.5:c.380T>C	ENSP00000467429.1:p.Met127Thr
ENST00000591179.5:c.773T>C	ENSP00000466800.1:p.Met258Thr
ENST00000591345.5:c.*872T>C	ENSP00000467313.1:n.*872T>C
NM_001302453.1:c.791T>C	NP_001289382.1:p.Met264Thr
NM_001302454.1:c.773T>C	NP_001289383.1:p.Met258Thr
NM_145045.4:c.953T>C	NP_659482.3:p.Met318Thr
XM_017026241.1:c.904+49T>C	XP_016881730.1:n.904+49T>C
NM_145045.5:c.953T>C MANE Select	NP_659482.3:p.Met318Thr
NM_001302454.2:c.773T>C	NP_001289383.1:p.Met258Thr