Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94942192G= , CM000672.2:g.94942192G= | GRCh38 |
| NC_000010.10:g.96701949G= , CM000672.1:g.96701949G= | GRCh37 |
| NC_000010.9:g.96691939G= | NCBI36 |
| NG_008385.1:g.8535G= | |
| NG_008385.2:g.9035G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000260682.8:c.332G= MANE Select | ENSP00000260682.6:p.Gly111= | |
| ENST00000643112.1:c.332G= | ENSP00000496202.1:p.Gly111= | |
| ENST00000645207.1:n.485G= | ||
| ENST00000260682.6:c.332G= | ENSP00000260682.6:p.Gly111= | |
| ENST00000461906.1:n.357G= | ||
| ENST00000473496.1:n.103G= | ||
| NM_000771.3:c.332G= | NP_000762.2:p.Gly111= | |
| NM_000771.4:c.332G= MANE Select | NP_000762.2:p.Gly111= |