Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10641465A>G , CM000682.2:g.10641465A>G | GRCh38 |
| NC_000020.10:g.10622113A>G , CM000682.1:g.10622113A>G | GRCh37 |
| NC_000020.9:g.10570113A>G | NCBI36 |
| NG_007496.1:g.37582T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000214.3:c.2911T>C MANE Select | NP_000205.1:p.Ser971Pro |
| ENST00000254958.10:c.2911T>C MANE Select | ENSP00000254958.4:p.Ser971Pro |
| NM_000214.2:c.2911T>C | NP_000205.1:p.Ser971Pro |
| ENST00000254958.9:c.2911T>C | ENSP00000254958.4:p.Ser971Pro |
| ENST00000423891.6:n.2777T>C |