Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.45405398C>T , CM000683.2:g.45405398C>T | GRCh38 |
| NC_000021.8:g.46825313C>T , CM000683.1:g.46825313C>T | GRCh37 |
| NC_000021.7:g.45649741C>T | NCBI36 |
| NG_011903.1:g.5217C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001379500.1:c.31C>T (COL18A1) MANE Select | NP_001366429.1:p.Arg11Trp |
| ENST00000651438.1:c.31C>T (COL18A1) MANE Select | ENSP00000498485.1:p.Arg11Trp |
| NM_130445.3:c.31C>T (COL18A1) | NP_569712.2:p.Arg11Trp |
| NM_130445.4:c.31C>T (COL18A1) | NP_569712.2:p.Arg11Trp |
| ENST00000400337.6:c.31C>T (COL18A1) | ENSP00000383191.2:p.Arg11Trp |
| XR_244333.2:n.45G>A (BNAT1) |