Canonical Allele Identifier: CA305327378

Gene: ODAD3

Linked Data

• dbSNP Id: rs141756170
• gnomAD v3: 19-11422931-C-A
• gnomAD v4: 19-11422931-C-A
• MyVariant Identifiers: chr19:g.11533599C>A (hg19) ; chr19:g.11422931C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11422931C>A , CM000681.2:g.11422931C>A	GRCh38
NC_000019.9:g.11533599C>A , CM000681.1:g.11533599C>A	GRCh37
NC_000019.8:g.11394599C>A	NCBI36
NG_041777.1:g.17852G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356392.9:c.1117-70G>T MANE Select	ENSP00000348757.3:n.1117-70G>T
ENST00000356392.8:c.1117-70G>T	ENSP00000348757.3:n.1117-70G>T
ENST00000586836.5:c.544-70G>T	ENSP00000467429.1:n.544-70G>T
ENST00000591179.5:c.937-70G>T	ENSP00000466800.1:n.937-70G>T
ENST00000591345.5:c.*1036-70G>T	ENSP00000467313.1:n.*1036-70G>T
NM_001302453.1:c.955-70G>T	NP_001289382.1:n.955-70G>T
NM_001302454.1:c.937-70G>T	NP_001289383.1:n.937-70G>T
NM_145045.4:c.1117-70G>T	NP_659482.3:n.1117-70G>T
XM_017026241.1:c.*11-70G>T	XP_016881730.1:n.*11-70G>T
NM_145045.5:c.1117-70G>T MANE Select	NP_659482.3:n.1117-70G>T
NM_001302454.2:c.937-70G>T	NP_001289383.1:n.937-70G>T