Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.202377521G= , CM000664.2:g.202377521G= | GRCh38 |
| NC_000002.11:g.203242244G= , CM000664.1:g.203242244G= | GRCh37 |
| NC_000002.10:g.202950489G= | NCBI36 |
| NG_009363.1:g.6195G= , LRG_712:g.6195G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001204.7:c.47G= MANE Select | NP_001195.2:p.Trp16= |
| ENST00000374580.10:c.47G= MANE Select | ENSP00000363708.4:p.Trp16= |
| NM_001204.6:c.47G= , LRG_712t1:c.47G= | NP_001195.2:p.Trp16= |
| ENST00000374574.2:c.47G= | ENSP00000363702.2:p.Trp16= |
| ENST00000374580.8:c.47G= | ENSP00000363708.4:p.Trp16= |
| XM_011511687.1:c.47G= | XP_011509989.1:p.Trp16= |
| XM_011511688.1:c.47G= | XP_011509990.1:p.Trp16= |