Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.38682852T= , CM000668.2:g.38682852T= | GRCh38 |
| NC_000006.11:g.38650628T= , CM000668.1:g.38650628T= | GRCh37 |
| NC_000006.10:g.38758606T= | NCBI36 |
| NG_012074.1:g.25325A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373365.5:c.332A= MANE Select | ENSP00000362463.3:p.Glu111= | |
| ENST00000373365.4:c.332A= | ENSP00000362463.3:p.Glu111= | |
| ENST00000470973.1:n.364A= | ||
| NM_006708.2:c.332A= | NP_006699.2:p.Glu111= | |
| NM_006708.3:c.332A= MANE Select | NP_006699.2:p.Glu111= |