Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153725346A>C , CM000685.2:g.153725346A>C | GRCh38 |
| NC_000023.10:g.152990801A>C , CM000685.1:g.152990801A>C | GRCh37 |
| NC_000023.9:g.152643995A>C | NCBI36 |
| NG_009022.2:g.5479A>C | |
| NG_023231.1:g.4401T>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000033.4:c.80A>C MANE Select | NP_000024.2:p.Tyr27Ser |
| ENST00000218104.6:c.80A>C MANE Select | ENSP00000218104.3:p.Tyr27Ser |
| NM_000033.3:c.80A>C | NP_000024.2:p.Tyr27Ser |
| ENST00000218104.5:c.80A>C | ENSP00000218104.3:p.Tyr27Ser |
| XR_938507.1:n.496A>C | |
| XR_938507.2:n.496A>C |