Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.30845253C= , CM000665.2:g.30845253C= | GRCh38 |
| NC_000003.11:g.30886745C= , CM000665.1:g.30886745C= | GRCh37 |
| NC_000003.10:g.30861749C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000282538.10:c.652-787G= MANE Select | ENSP00000282538.5:n.652-787G= | |
| ENST00000282538.9:c.652-787G= | ENSP00000282538.5:n.652-787G= | |
| ENST00000454381.3:c.652-787G= | ENSP00000427059.1:n.652-787G= | |
| NM_207359.2:c.652-787G= | NP_997242.2:n.652-787G= | |
| XM_017006297.1:c.595-787G= | XP_016861786.1:n.595-787G= | |
| XM_017006298.1:c.-7-989G= | XP_016861787.1:n.-7-989G= | |
| NM_207359.3:c.652-787G= MANE Select | NP_997242.2:n.652-787G= |