Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.28812463G>C , CM000663.2:g.28812463G>C | GRCh38 |
| NC_000001.10:g.29138975G>C , CM000663.1:g.29138975G>C | GRCh37 |
| NC_000001.9:g.29011562G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000911.4:c.80G>C MANE Select | NP_000902.3:p.Cys27Ser |
| ENST00000234961.7:c.80G>C MANE Select | ENSP00000234961.2:p.Cys27Ser |
| NM_000911.3:c.80G>C | NP_000902.3:p.Cys27Ser |
| ENST00000234961.6:c.80G>C | ENSP00000234961.2:p.Cys27Ser |
| ENST00000621425.1:c.80G>C | ENSP00000477970.1:p.Cys27Ser |