Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.44456833G= , CM000683.2:g.44456833G= | GRCh38 |
| NC_000021.8:g.45876716G= , CM000683.1:g.45876716G= | GRCh37 |
| NC_000021.7:g.44701144G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_030891.6:c.189G= MANE Select | NP_112153.1:p.Pro63= |
| ENST00000291592.6:c.189G= MANE Select | ENSP00000291592.4:p.Pro63= |
| NM_030891.4:c.189G= | NP_112153.1:p.Pro63= |
| NM_030891.5:c.189G= | NP_112153.1:p.Pro63= |
| ENST00000291592.5:c.189G= | ENSP00000291592.4:p.Pro63= |