Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.63127421C= , CM000680.2:g.63127421C= | GRCh38 |
| NC_000018.9:g.60794654C= , CM000680.1:g.60794654C= | GRCh37 |
| NC_000018.8:g.58945634C= | NCBI36 |
| NG_009361.1:g.196960G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000633.3:c.*1204G= MANE Select | NP_000624.2:n.*1204G= |
| ENST00000333681.5:c.*1204G= MANE Select | ENSP00000329623.3:n.*1204G= |
| NM_000633.2:c.*1204G= | NP_000624.2:n.*1204G= |
| ENST00000333681.4:c.*1204G= | ENSP00000329623.3:n.*1204G= |
| ENST00000398117.1:c.*1204G= | ENSP00000381185.1:n.*1204G= |
| ENST00000677635.1:n.1488G= | |
| ENST00000678134.1:c.2128G= | ENSP00000503628.1:n.2128G= |
| ENST00000678301.1:c.*1204G= | ENSP00000504546.1:n.*1204G= |
| ENST00000678349.1:c.2476G= | ENSP00000504190.1:n.2476G= |