Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.17053906T= , CM000663.2:g.17053906T= | GRCh38 |
| NC_000001.10:g.17380401T= , CM000663.1:g.17380401T= | GRCh37 |
| NC_000001.9:g.17252988T= | NCBI36 |
| NG_012340.1:g.5265A= , LRG_316:g.5265A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375499.8:c.72+42A= MANE Select | ENSP00000364649.3:n.72+42A= | |
| ENST00000375499.7:c.72+42A= | ENSP00000364649.3:n.72+42A= | |
| ENST00000466613.2:n.84+42A= | ||
| ENST00000485515.5:n.60+42A= | ||
| NM_003000.2:c.72+42A= , LRG_316t1:c.72+42A= | NP_002991.2:n.72+42A= | |
| NM_003000.3:c.72+42A= MANE Select | NP_002991.2:n.72+42A= |