Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.37803927C>T , CM000665.2:g.37803927C>T | GRCh38 |
| NC_000003.11:g.37845418C>T , CM000665.1:g.37845418C>T | GRCh37 |
| NC_000003.10:g.37820422C>T | NCBI36 |
| NG_016166.1:g.356606C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264741.10:c.2994C>T (ITGA9) MANE Select | ENSP00000264741.5:p.Ala998= | |
| ENST00000264741.9:c.2994C>T (ITGA9) | ENSP00000264741.5:p.Ala998= | |
| ENST00000411817.2:c.110-14964C>T (ITGA9) | ||
| NM_002207.2:c.2994C>T (ITGA9) | NP_002198.2:p.Ala998= | |
| NR_110531.1:n.256+17087G>A (ITGA9-AS1) | ||
| NR_110532.1:n.326-13016G>A (ITGA9-AS1) | ||
| NM_002207.3:c.2994C>T (ITGA9) MANE Select | NP_002198.2:p.Ala998= |