Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48380208T= , CM000675.2:g.48380208T= | GRCh38 |
| NC_000013.10:g.48954344T= , CM000675.1:g.48954344T= | GRCh37 |
| NC_000013.9:g.47852345T= | NCBI36 |
| NG_009009.1:g.81462T= , LRG_517:g.81462T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000267163.6:c.1465T= MANE Select | ENSP00000267163.4:p.Cys489= | |
| ENST00000650461.1:c.1465T= | ENSP00000497193.1:p.Cys489= | |
| ENST00000267163.4:c.1465T= | ENSP00000267163.4:p.Cys489= | |
| NM_000321.2:c.1465T= , LRG_517t1:c.1465T= | NP_000312.2:p.Cys489= | |
| XM_011535171.1:c.1204T= | XP_011533473.1:p.Cys402= | |
| XM_011535171.2:c.1204T= | XP_011533473.1:p.Cys402= | |
| NM_000321.3:c.1465T= MANE Select | NP_000312.2:p.Cys489= |