Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.23573281A= , CM000684.2:g.23573281A= | GRCh38 |
| NC_000022.10:g.23915468A= , CM000684.1:g.23915468A= | GRCh37 |
| NC_000022.9:g.22245468A= | NCBI36 |
| NG_009791.1:g.12028T= , LRG_69:g.12028T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000330377.3:c.627T= MANE Select | ENSP00000329312.2:p.Pro209= | |
| ENST00000249053.3:c.*256T= | ENSP00000249053.3:n.*256T= | |
| ENST00000330377.2:c.627T= | ENSP00000329312.2:p.Pro209= | |
| NM_020070.3:c.627T= | NP_064455.1:p.Pro209= | |
| NM_152855.2:c.*256T= | NP_690594.1:n.*256T= | |
| XM_011530169.1:c.630T= | XP_011528471.1:p.Pro210= | |
| XM_011530169.2:c.630T= | XP_011528471.1:p.Pro210= | |
| NM_020070.4:c.627T= MANE Select | NP_064455.1:p.Pro209= | |
| NM_001369906.1:c.630T= | NP_001356835.1:p.Pro210= | |
| NM_152855.3:c.*256T= | NP_690594.1:n.*256T= |