Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.233618524G= , CM000664.2:g.233618524G= | GRCh38 |
| NC_000002.11:g.234527170G= , CM000664.1:g.234527170G= | GRCh37 |
| NC_000002.10:g.234191909G= | NCBI36 |
| NG_002601.2:g.33781G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373450.5:c.817G= MANE Select | ENSP00000362549.4:p.Gly273= | |
| ENST00000373450.4:c.817G= | ENSP00000362549.4:p.Gly273= | |
| NM_019076.4:c.817G= | NP_061949.3:p.Gly273= | |
| NM_019076.5:c.817G= MANE Select | NP_061949.3:p.Gly273= |