Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.3154825T= , CM000668.2:g.3154825T= | GRCh38 |
| NC_000006.11:g.3155059T= , CM000668.1:g.3155059T= | GRCh37 |
| NC_000006.10:g.3100058T= | NCBI36 |
| NG_042223.1:g.7725A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000333628.4:c.376A= MANE Select | ENSP00000369703.2:p.Ser126= | |
| ENST00000679400.1:n.432A= | ||
| ENST00000679907.1:n.764A= | ||
| ENST00000680036.1:n.1158A= | ||
| ENST00000680967.1:n.1466A= | ||
| ENST00000333628.3:c.376A= | ENSP00000369703.2:p.Ser126= | |
| ENST00000489942.1:n.571A= | ||
| NM_001069.2:c.376A= | NP_001060.1:p.Ser126= | |
| NM_001310315.1:c.121A= | NP_001297244.1:p.Ser41= | |
| NM_001069.3:c.376A= MANE Select | NP_001060.1:p.Ser126= | |
| NM_001310315.2:c.121A= | NP_001297244.1:p.Ser41= |