Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.39247938G= , CM000681.2:g.39247938G= | GRCh38 |
| NC_000019.9:g.39738578G= , CM000681.1:g.39738578G= | GRCh37 |
| NC_000019.8:g.44430418G= | NCBI36 |
| NG_042193.1:g.2034C= | |
| NG_055295.1:g.5919C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NR_074079.1:n.486C= | |
| ENST00000606380.2:c.209C= | ENSP00000476098.1:p.Ser70= |
| ENST00000610963.1:c.208C= | ENSP00000481371.1:p.Pro70= |
| ENST00000616270.4:c.209C= | ENSP00000480679.1:p.Ser70= |
| ENST00000634680.1:c.152-475C= | ENSP00000489240.1:n.152-475C= |
| ENST00000634967.1:c.209C= | ENSP00000489559.1:p.Ser70= |