Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94780643G= , CM000672.2:g.94780643G= | GRCh38 |
| NC_000010.10:g.96540400G= , CM000672.1:g.96540400G= | GRCh37 |
| NC_000010.9:g.96530390G= | NCBI36 |
| NG_008384.2:g.22938G= | |
| NG_008384.3:g.22963G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371321.9:c.626G= MANE Select | ENSP00000360372.3:p.Ser209= | |
| ENST00000645461.1:n.1679G= | ||
| ENST00000371321.7:c.626G= | ENSP00000360372.3:p.Ser209= | |
| ENST00000464755.1:c.1389G= | ENSP00000483243.1:n.1389G= | |
| NM_000769.2:c.626G= | NP_000760.1:p.Ser209= | |
| NM_000769.4:c.626G= MANE Select | NP_000760.1:p.Ser209= |