Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.1985994G= , CM000678.2:g.1985994G= | GRCh38 |
| NC_000016.9:g.2035995G= , CM000678.1:g.2035995G= | GRCh37 |
| NC_000016.8:g.1975996G= | NCBI36 |
| NG_016288.1:g.6846G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000567719.2:c.359G= | ENSP00000455885.1:p.Trp120= | |
| ENST00000248114.7:c.584G= MANE Select | ENSP00000248114.6:p.Trp195= | |
| ENST00000248114.6:c.584G= | ENSP00000248114.6:p.Trp195= | |
| ENST00000565658.1:n.741G= | ||
| ENST00000567719.1:c.359G= | ENSP00000455885.1:p.Trp120= | |
| ENST00000569451.1:c.*57G= | ENSP00000456432.1:n.*57G= | |
| NM_005262.2:c.584G= | NP_005253.3:p.Trp195= | |
| NM_005262.3:c.584G= MANE Select | NP_005253.3:p.Trp195= |