Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.23418781A>C , CM000678.2:g.23418781A>C | GRCh38 |
| NC_000016.9:g.23430102A>C , CM000678.1:g.23430102A>C | GRCh37 |
| NC_000016.8:g.23337603A>C | NCBI36 |
| NG_021287.1:g.39411T>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_153603.4:c.1056T>G MANE Select | NP_705831.1:p.Tyr352Ter |
| ENST00000307149.10:c.1056T>G MANE Select | ENSP00000305442.5:p.Tyr352Ter |
| NM_153603.3:c.1056T>G | NP_705831.1:p.Tyr352Ter |
| ENST00000307149.9:c.1056T>G | ENSP00000305442.5:p.Tyr352Ter |
| XM_017023870.1:c.861T>G | XP_016879359.1:p.Tyr287Ter |
| XR_002957852.1:n.1277T>G | |
| XR_429680.1:n.1272T>G | |
| XR_429680.2:n.1277T>G |