Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.74919892A= , CM000679.2:g.74919892A= | GRCh38 |
| NC_000017.10:g.72915987A= , CM000679.1:g.72915987A= | GRCh37 |
| NC_000017.9:g.70427582A= | NCBI36 |
| NG_007882.1:g.8365T= | |
| NG_033062.1:g.618A= | |
| NG_007882.2:g.8372T= | |
| NG_033062.2:g.618A= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000614341.5:c.944T= MANE Select | ENSP00000480279.1:p.Met315= | |
| ENST00000579243.1:c.*543T= | ENSP00000462568.1:n.*543T= | |
| ENST00000614341.4:c.944T= | ENSP00000480279.1:p.Met315= | |
| NM_001282489.2:c.635T= | NP_001269418.1:p.Met212= | |
| NM_173477.4:c.944T= | NP_775748.2:p.Met315= | |
| XM_011524296.1:c.635T= | XP_011522598.1:p.Met212= | |
| XM_011524296.2:c.635T= | XP_011522598.1:p.Met212= | |
| NM_173477.5:c.944T= MANE Select | NP_775748.2:p.Met315= | |
| NM_001282489.3:c.635T= | NP_001269418.1:p.Met212= |