Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.228744368G= , CM000663.2:g.228744368G= | GRCh38 |
| NC_000001.10:g.228880115G= , CM000663.1:g.228880115G= | GRCh37 |
| NC_000001.9:g.226946738G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000366691.4:c.*628G= MANE Select | ENSP00000355652.3:n.*628G= | |
| ENST00000366691.3:c.*628G= | ENSP00000355652.3:n.*628G= | |
| NM_021205.5:c.*628G= | NP_067028.1:n.*628G= | |
| NR_037962.1:n.1529G= | ||
| NM_021205.6:c.*628G= MANE Select | NP_067028.1:n.*628G= |