Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.204161401G>C , CM000663.2:g.204161401G>C | GRCh38 |
| NC_000001.10:g.204130529G>C , CM000663.1:g.204130529G>C | GRCh37 |
| NC_000001.9:g.202397152G>C | NCBI36 |
| NG_012122.1:g.9937C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272190.9:c.264C>G MANE Select | ENSP00000272190.8:p.Gly88= | |
| ENST00000638118.1:c.150C>G | ENSP00000490307.1:p.Gly50= | |
| ENST00000272190.8:c.264C>G | ENSP00000272190.8:p.Gly88= | |
| NM_000537.3:c.264C>G | NP_000528.1:p.Gly88= | |
| NM_000537.4:c.264C>G MANE Select | NP_000528.1:p.Gly88= |