Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.149926377T= , CM000663.2:g.149926377T= | GRCh38 |
| NC_000001.10:g.149898269T= , CM000663.1:g.149898269T= | GRCh37 |
| NC_000001.9:g.148164893T= | NCBI36 |
| NG_032777.1:g.6876A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271628.9:c.705A= MANE Select | ENSP00000271628.8:p.Pro235= | |
| ENST00000271628.8:c.705A= | ENSP00000271628.8:p.Pro235= | |
| NM_005850.4:c.705A= | NP_005841.1:p.Pro235= | |
| NM_005850.5:c.705A= MANE Select | NP_005841.1:p.Pro235= |