Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.226795828C= , CM000664.2:g.226795828C= | GRCh38 |
| NC_000002.11:g.227660544C= , CM000664.1:g.227660544C= | GRCh37 |
| NC_000002.10:g.227368788C= | NCBI36 |
| NG_015830.1:g.7963G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000305123.6:c.2911G= MANE Select | ENSP00000304895.4:p.Gly971= | |
| ENST00000305123.5:c.2911G= | ENSP00000304895.4:p.Gly971= | |
| NM_005544.2:c.2911G= | NP_005535.1:p.Gly971= | |
| NM_005544.3:c.2911G= MANE Select | NP_005535.1:p.Gly971= |