Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.101830823C= , CM000674.2:g.101830823C= | GRCh38 |
| NC_000012.11:g.102224601C= , CM000674.1:g.102224601C= | GRCh37 |
| NC_000012.10:g.100748732C= | NCBI36 |
| NG_021243.1:g.5045G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299314.12:c.-148G= MANE Select | ENSP00000299314.7:n.-148G= | |
| ENST00000299314.11:c.-148G= | ENSP00000299314.7:n.-148G= | |
| ENST00000392919.4:c.-148G= | ENSP00000376651.4:n.-148G= | |
| NM_024312.4:c.-148G= | NP_077288.2:n.-148G= | |
| XM_006719593.2:c.-148G= | XP_006719656.1:n.-148G= | |
| XM_017019961.1:c.-297G= | XP_016875450.1:n.-297G= | |
| NM_024312.5:c.-148G= MANE Select | NP_077288.2:n.-148G= |