Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.202555502A>G , CM000664.2:g.202555502A>G | GRCh38 |
| NC_000002.11:g.203420225A>G , CM000664.1:g.203420225A>G | GRCh37 |
| NC_000002.10:g.203128470A>G | NCBI36 |
| NG_009363.1:g.184176A>G , LRG_712:g.184176A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001204.7:c.1837A>G MANE Select | NP_001195.2:p.Thr613Ala |
| ENST00000374580.10:c.1837A>G MANE Select | ENSP00000363708.4:p.Thr613Ala |
| NM_001204.6:c.1837A>G , LRG_712t1:c.1837A>G | NP_001195.2:p.Thr613Ala |
| ENST00000374574.2:c.1586+2614A>G | ENSP00000363702.2:n.1586+2614A>G |
| ENST00000374580.8:c.1837A>G | ENSP00000363708.4:p.Thr613Ala |
| ENST00000638587.1:c.1768A>G | ENSP00000491062.1:n.1768A>G |
| XM_011511687.1:c.1837A>G | XP_011509989.1:p.Thr613Ala |
| XM_011511688.1:c.1586+2614A>G | XP_011509990.1:n.1586+2614A>G |