Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.25012937G= , CM000685.2:g.25012937G= | GRCh38 |
| NC_000023.10:g.25031054G= , CM000685.1:g.25031054G= | GRCh37 |
| NC_000023.9:g.24940975G= | NCBI36 |
| NG_008281.1:g.8012C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_139058.3:c.1058C= MANE Select | NP_620689.1:p.Pro353= |
| ENST00000379044.5:c.1058C= MANE Select | ENSP00000368332.4:p.Pro353= |
| NM_139058.2:c.1058C= | NP_620689.1:p.Pro353= |
| ENST00000379044.4:c.1058C= | ENSP00000368332.4:p.Pro353= |