Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.86743617G= , CM000670.2:g.86743617G= | GRCh38 |
| NC_000008.10:g.87755845G= , CM000670.1:g.87755845G= | GRCh37 |
| NC_000008.9:g.87824961G= | NCBI36 |
| NG_016980.1:g.5059C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_019098.5:c.11C= MANE Select | NP_061971.3:p.Ser4= |
| ENST00000320005.6:c.11C= MANE Select | ENSP00000316605.5:p.Ser4= |
| NM_019098.4:c.11C= | NP_061971.3:p.Ser4= |
| ENST00000320005.5:c.11C= | ENSP00000316605.5:p.Ser4= |
| ENST00000681746.1:c.11C= | ENSP00000505959.1:p.Ser4= |