Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.37813623C>T , CM000665.2:g.37813623C>T | GRCh38 |
| NC_000003.11:g.37855114C>T , CM000665.1:g.37855114C>T | GRCh37 |
| NC_000003.10:g.37830118C>T | NCBI36 |
| NG_016166.1:g.366302C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002207.3:c.3010-5268C>T (ITGA9) MANE Select | NP_002198.2:n.3010-5268C>T |
| ENST00000264741.10:c.3010-5268C>T (ITGA9) MANE Select | ENSP00000264741.5:n.3010-5268C>T |
| NM_002207.2:c.3010-5268C>T (ITGA9) | NP_002198.2:n.3010-5268C>T |
| NR_110531.1:n.256+7391G>A (ITGA9-AS1) | |
| NR_110532.1:n.325+7391G>A (ITGA9-AS1) | |
| ENST00000264741.9:c.3010-5268C>T (ITGA9) | ENSP00000264741.5:n.3010-5268C>T |
| ENST00000411817.2:c.110-5268C>T (ITGA9) |