Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.4860357C= , CM000666.2:g.4860357C= | GRCh38 |
| NC_000004.11:g.4862084C= , CM000666.1:g.4862084C= | GRCh37 |
| NC_000004.10:g.4912985C= | NCBI36 |
| NG_008121.1:g.5693C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002448.3:c.458C= MANE Select | NP_002439.2:p.Pro153= |
| ENST00000382723.5:c.458C= MANE Select | ENSP00000372170.4:p.Pro153= |
| ENST00000382723.4:c.458C= | ENSP00000372170.4:p.Pro153= |