Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.152660756A>C , CM000669.2:g.152660756A>C | GRCh38 |
| NC_000007.13:g.152357841A>C , CM000669.1:g.152357841A>C | GRCh37 |
| NC_000007.12:g.151988774A>C | NCBI36 |
| NG_027988.1:g.20410T>G | |
| NG_027988.2:g.20410T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000698506.1:c.-47-11393T>G | ENSP00000513758.1:n.-47-11393T>G | |
| ENST00000698507.1:n.134T>G | ||
| ENST00000359321.2:c.66T>G MANE Select | ENSP00000352271.1:p.Ser22Arg | |
| ENST00000359321.1:c.66T>G | ENSP00000352271.1:p.Ser22Arg | |
| ENST00000495707.1:n.88T>G | ||
| NM_005431.1:c.66T>G | NP_005422.1:p.Ser22Arg | |
| NM_005431.2:c.66T>G MANE Select | NP_005422.1:p.Ser22Arg |