Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.64616100G= , CM000670.2:g.64616100G= | GRCh38 |
| NC_000008.10:g.65528657G= , CM000670.1:g.65528657G= | GRCh37 |
| NC_000008.9:g.65691211G= | NCBI36 |
| NG_008338.1:g.187692C= | |
| NG_008338.2:g.187692C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000310193.4:c.441C= MANE Select | ENSP00000310721.3:p.Gly147= | |
| ENST00000310193.3:c.441C= | ENSP00000310721.3:p.Gly147= | |
| NM_004820.3:c.441C= | NP_004811.1:p.Gly147= | |
| NM_001324112.1:c.441C= | NP_001311041.1:p.Gly147= | |
| NM_004820.4:c.441C= | NP_004811.1:p.Gly147= | |
| XM_017014002.1:c.507C= | XP_016869491.1:p.Gly169= | |
| NM_004820.5:c.441C= MANE Select | NP_004811.1:p.Gly147= | |
| NM_001324112.2:c.441C= | NP_001311041.1:p.Gly147= |