Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.10874619A>G , CM000668.2:g.10874619A>G | GRCh38 |
| NC_000006.11:g.10874852A>G , CM000668.1:g.10874852A>G | GRCh37 |
| NC_000006.10:g.10982838A>G | NCBI36 |
| NG_008970.1:g.12247T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379491.5:c.897T>C MANE Select | ENSP00000368805.4:p.Pro299= | |
| ENST00000379491.4:c.897T>C | ENSP00000368805.4:p.Pro299= | |
| ENST00000480294.1:c.101-16894A>G | ENSP00000417929.1:n.101-16894A>G | |
| NM_004752.3:c.897T>C | NP_004743.1:p.Pro299= | |
| XM_011514991.1:c.897T>C | XP_011513293.1:p.Pro299= | |
| NM_004752.4:c.897T>C MANE Select | NP_004743.1:p.Pro299= |