Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.29313161C= , CM000684.2:g.29313161C= | GRCh38 |
| NC_000022.10:g.29709150C= , CM000684.1:g.29709150C= | GRCh37 |
| NC_000022.9:g.28039150C= | NCBI36 |
| NG_032959.1:g.11155C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216101.7:c.*140G= MANE Select | ENSP00000216101.6:n.*140G= | |
| ENST00000216101.6:c.*140G= | ENSP00000216101.6:n.*140G= | |
| ENST00000401450.3:c.*698G= | ENSP00000386095.3:n.*698G= | |
| NM_006477.4:c.*140G= | NP_006468.1:n.*140G= | |
| XM_011529821.1:c.*140G= | XP_011528123.1:n.*140G= | |
| XM_011529822.1:c.*140G= | XP_011528124.1:n.*140G= | |
| XM_011529823.1:c.*140G= | XP_011528125.1:n.*140G= | |
| NM_006477.5:c.*140G= MANE Select | NP_006468.1:n.*140G= |