Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.50910091T>C , CM000676.2:g.50910091T>C | GRCh38 |
| NC_000014.8:g.51376809T>C , CM000676.1:g.51376809T>C | GRCh37 |
| NC_000014.7:g.50446559T>C | NCBI36 |
| NG_012796.1:g.39440A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002863.5:c.1981A>G MANE Select | NP_002854.3:p.Thr661Ala |
| ENST00000216392.8:c.1981A>G MANE Select | ENSP00000216392.7:p.Thr661Ala |
| NM_001163940.1:c.1879A>G | NP_001157412.1:p.Thr627Ala |
| NM_001163940.2:c.1879A>G | NP_001157412.1:p.Thr627Ala |
| NM_002863.4:c.1981A>G | NP_002854.3:p.Thr661Ala |
| ENST00000216392.7:c.1981A>G | ENSP00000216392.7:p.Thr661Ala |
| ENST00000532107.2:n.154A>G | |
| ENST00000532462.5:c.1981A>G | ENSP00000431657.1:p.Thr661Ala |
| ENST00000544180.6:c.1879A>G | ENSP00000443787.1:p.Thr627Ala |