Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31535386C>G , CM000680.2:g.31535386C>G | GRCh38 |
| NC_000018.9:g.29115349C>G , CM000680.1:g.29115349C>G | GRCh37 |
| NC_000018.8:g.27369347C>G | NCBI36 |
| NG_007072.3:g.42145C>G , LRG_397:g.42145C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000261590.13:c.1397C>G MANE Select | ENSP00000261590.8:p.Thr466Ser | |
| ENST00000261590.12:c.1397C>G | ENSP00000261590.8:p.Thr466Ser | |
| NM_001943.3:c.1397C>G , LRG_397t1:c.1397C>G | NP_001934.2:p.Thr466Ser | |
| NM_001943.4:c.1397C>G | NP_001934.2:p.Thr466Ser | |
| XM_024451095.1:c.863C>G | XP_024306863.1:p.Thr288Ser | |
| NM_001943.5:c.1397C>G MANE Select | NP_001934.2:p.Thr466Ser |