Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.168293216G= , CM000663.2:g.168293216G= | GRCh38 |
| NC_000001.10:g.168262454G= , CM000663.1:g.168262454G= | GRCh37 |
| NC_000001.9:g.166529078G= | NCBI36 |
| NG_008244.1:g.17177G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000367821.8:c.541G= MANE Select | ENSP00000356795.3:p.Val181= | |
| ENST00000367821.7:c.541G= | ENSP00000356795.3:p.Val181= | |
| ENST00000431969.5:c.338G= | ||
| NM_005149.2:c.541G= | NP_005140.1:p.Val181= | |
| NM_005149.3:c.541G= MANE Select | NP_005140.1:p.Val181= |