Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67436142G>C , CM000678.2:g.67436142G>C | GRCh38 |
| NC_000016.9:g.67470045G>C , CM000678.1:g.67470045G>C | GRCh37 |
| NC_000016.8:g.66027546G>C | NCBI36 |
| NG_011482.1:g.50045C>G | |
| NG_016549.1:g.10010G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000326152.6:c.664G>C MANE Select | ENSP00000316786.5:p.Gly222Arg | |
| ENST00000326152.5:c.664G>C | ENSP00000316786.5:p.Gly222Arg | |
| ENST00000567684.2:n.527G>C | ||
| NM_000196.3:c.664G>C | NP_000187.3:p.Gly222Arg | |
| NM_000196.4:c.664G>C MANE Select | NP_000187.3:p.Gly222Arg |