Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.17134505C>T , CM000678.2:g.17134505C>T | GRCh38 |
| NC_000016.9:g.17228362C>T , CM000678.1:g.17228362C>T | GRCh37 |
| NC_000016.8:g.17135863C>T | NCBI36 |
| NG_015843.1:g.341377G>A | |
| NG_015843.2:g.341377G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_022166.4:c.1995G>A MANE Select | NP_071449.1:p.Thr665= |
| ENST00000261381.7:c.1995G>A MANE Select | ENSP00000261381.6:p.Thr665= |
| NM_022166.3:c.1995G>A | NP_071449.1:p.Thr665= |
| NR_135179.1:n.2C>T | |
| ENST00000261381.6:c.1995G>A | ENSP00000261381.6:p.Thr665= |
| XM_011522574.1:c.1995G>A | XP_011520876.1:p.Thr665= |
| XM_017023539.2:c.1995G>A | XP_016879028.1:p.Thr665= |
| XM_017023540.2:c.1995G>A | XP_016879029.1:p.Thr665= |
| XR_933140.1:n.37C>T | |
| XR_933141.1:n.30C>T | |
| XR_933143.1:n.37C>T |