ClinVar

NM_002207.3(ITGA9):c.2667+32G>A

Genes:

ITGA9-AS1:ITGA9 antisense RNA 1 [Gene - HGNC]
ITGA9:integrin subunit alpha 9 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

3p22.2

Genomic location:

• Chr3: 37777549 (on Assembly GRCh38)
• Chr3: 37819040 (on Assembly GRCh37)

Preferred name:

NM_002207.3(ITGA9):c.2667+32G>A

HGVS:

• NC_000003.12:g.37777549G>A
• NG_016166.1:g.330228G>A
• NM_002207.3:c.2667+32G>AMANE SELECT
• NC_000003.11:g.37819040G>A
• NM_002207.2:c.2667+32G>A

This HGVS expression did not pass validation

Links:

dbSNP: rs76424398

NCBI 1000 Genomes Browser:

rs76424398

Molecular consequence:

• NM_002207.3:c.2667+32G>A - intron variant - [Sequence Ontology: SO:0001627]

Observations:

1