Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.86954989G= , CM000673.2:g.86954989G= | GRCh38 |
| NC_000011.9:g.86666031G= , CM000673.1:g.86666031G= | GRCh37 |
| NC_000011.8:g.86343679G= | NCBI36 |
| NG_011752.1:g.5403C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000531380.2:c.97C= MANE Select | ENSP00000434034.1:p.Pro33= | |
| ENST00000531380.1:c.97C= | ENSP00000434034.1:p.Pro33= | |
| NM_012193.3:c.97C= | NP_036325.2:p.Pro33= | |
| NM_012193.4:c.97C= MANE Select | NP_036325.2:p.Pro33= |