Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.167789149C= , CM000665.2:g.167789149C= | GRCh38 |
| NC_000003.11:g.167506937C= , CM000665.1:g.167506937C= | GRCh37 |
| NC_000003.10:g.168989631C= | NCBI36 |
| NG_008217.1:g.58506C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001122752.2:c.21C= MANE Select | NP_001116224.1:p.Phe7= |
| ENST00000446050.7:c.21C= MANE Select | ENSP00000397373.2:p.Phe7= |
| NM_001122752.1:c.21C= | NP_001116224.1:p.Phe7= |
| NM_005025.4:c.21C= | NP_005016.1:p.Phe7= |
| NM_005025.5:c.21C= | NP_005016.1:p.Phe7= |
| ENST00000295777.9:c.21C= | ENSP00000295777.5:p.Phe7= |
| ENST00000446050.6:c.21C= | ENSP00000397373.2:p.Phe7= |
| ENST00000472747.2:c.21C= | ENSP00000420561.2:p.Phe7= |
| ENST00000472941.5:c.21C= | ENSP00000420133.1:p.Phe7= |
| XM_017006618.2:c.21C= | XP_016862107.1:p.Phe7= |