Canonical Allele Identifier: CA305327083
Gene: ODAD3 HGNC NCBI

Linked Data

dbSNP Id: rs975032611
gnomAD v4: 19-11422655-G-C
MyVariant Identifiers: chr19:g.11533323G>C (hg19) chr19:g.11422655G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11422655G>C , CM000681.2:g.11422655G>C GRCh38
NC_000019.9:g.11533323G>C , CM000681.1:g.11533323G>C GRCh37
NC_000019.8:g.11394323G>C NCBI36
NG_041777.1:g.18128C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356392.9:c.1278-28C>G MANE Select ENSP00000348757.3:n.1278-28C>G
ENST00000356392.8:c.1278-28C>G ENSP00000348757.3:n.1278-28C>G
ENST00000586836.5:c.705-28C>G ENSP00000467429.1:n.705-28C>G
ENST00000591179.5:c.1098-28C>G ENSP00000466800.1:n.1098-28C>G
ENST00000591345.5:c.*1197-28C>G ENSP00000467313.1:n.*1197-28C>G
NM_001302453.1:c.1116-28C>G NP_001289382.1:n.1116-28C>G
NM_001302454.1:c.1098-28C>G NP_001289383.1:n.1098-28C>G
NM_145045.4:c.1278-28C>G NP_659482.3:n.1278-28C>G
NM_145045.5:c.1278-28C>G MANE Select NP_659482.3:n.1278-28C>G
NM_001302454.2:c.1098-28C>G NP_001289383.1:n.1098-28C>G
Search 100 bp 5'
Search 100 bp 3'