Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.5023573C= , CM000679.2:g.5023573C= | GRCh38 |
| NC_000017.10:g.4926868C= , CM000679.1:g.4926868C= | GRCh37 |
| NC_000017.9:g.4867592C= | NCBI36 |
| NG_034137.1:g.30626C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006612.6:c.2734C= MANE Select | NP_006603.2:p.Arg912= |
| ENST00000320785.10:c.2734C= MANE Select | ENSP00000320821.5:p.Arg912= |
| NM_006612.5:c.2734C= | NP_006603.2:p.Arg912= |
| ENST00000320785.9:c.2734C= | ENSP00000320821.5:p.Arg912= |
| XM_005256424.1:c.2734C= | XP_005256481.1:p.Arg912= |
| XM_005256424.2:c.2734C= | XP_005256481.1:p.Arg912= |