Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.233618421T= , CM000664.2:g.233618421T= | GRCh38 |
| NC_000002.11:g.234527067T= , CM000664.1:g.234527067T= | GRCh37 |
| NC_000002.10:g.234191806T= | NCBI36 |
| NG_002601.2:g.33678T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373450.5:c.714T= MANE Select | ENSP00000362549.4:p.Pro238= | |
| ENST00000373450.4:c.714T= | ENSP00000362549.4:p.Pro238= | |
| NM_019076.4:c.714T= | NP_061949.3:p.Pro238= | |
| NM_019076.5:c.714T= MANE Select | NP_061949.3:p.Pro238= |