Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154187840C= , CM000685.2:g.154187840C= | GRCh38 |
| NC_000023.10:g.153453329C= , CM000685.1:g.153453329C= | GRCh37 |
| NG_011606.1:g.10245C= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000595290.6:c.183C= MANE Select | ENSP00000472316.1:p.Ile61= | |
| ENST00000595290.5:c.183C= | ENSP00000472316.1:p.Ile61= | |
| ENST00000595330.1:n.193C= | ||
| NM_000513.2:c.183C= MANE Select | NP_000504.1:p.Ile61= |