Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.37785077C>T , CM000665.2:g.37785077C>T | GRCh38 |
| NC_000003.11:g.37826568C>T , CM000665.1:g.37826568C>T | GRCh37 |
| NC_000003.10:g.37801572C>T | NCBI36 |
| NG_016166.1:g.337756C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264741.10:c.2888C>T (ITGA9) MANE Select | ENSP00000264741.5:p.Thr963Met | |
| ENST00000264741.9:c.2888C>T (ITGA9) | ENSP00000264741.5:p.Thr963Met | |
| ENST00000411817.2:c.108C>T (ITGA9) | ||
| NM_002207.2:c.2888C>T (ITGA9) | NP_002198.2:p.Thr963Met | |
| NR_110531.1:n.257-31025G>A (ITGA9-AS1) | ||
| NM_002207.3:c.2888C>T (ITGA9) MANE Select | NP_002198.2:p.Thr963Met |