Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94775175G>A , CM000672.2:g.94775175G>A | GRCh38 |
| NC_000010.10:g.96534932G>A , CM000672.1:g.96534932G>A | GRCh37 |
| NC_000010.9:g.96524922G>A | NCBI36 |
| NG_008384.2:g.17470G>A | |
| NG_008384.3:g.17495G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371321.9:c.286G>A MANE Select | ENSP00000360372.3:p.Gly96Arg | |
| ENST00000645461.1:n.1339G>A | ||
| ENST00000371321.7:c.286G>A | ENSP00000360372.3:p.Gly96Arg | |
| ENST00000464755.1:c.1049G>A | ENSP00000483243.1:n.1049G>A | |
| ENST00000480405.2:c.286G>A | ENSP00000483847.1:p.Gly96Arg | |
| NM_000769.2:c.286G>A | NP_000760.1:p.Gly96Arg | |
| NM_000769.4:c.286G>A MANE Select | NP_000760.1:p.Gly96Arg |