Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8009531T= , CM000679.2:g.8009531T= | GRCh38 |
| NC_000017.10:g.7912849T= , CM000679.1:g.7912849T= | GRCh37 |
| NC_000017.9:g.7853574T= | NCBI36 |
| NG_009092.1:g.11862T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000180.4:c.1694T= MANE Select | NP_000171.1:p.Phe565= |
| ENST00000254854.5:c.1694T= MANE Select | ENSP00000254854.4:p.Phe565= |
| NM_000180.3:c.1694T= | NP_000171.1:p.Phe565= |
| ENST00000254854.4:c.1694T= | ENSP00000254854.4:p.Phe565= |
| XM_011523816.1:c.1694T= | XP_011522118.1:p.Phe565= |