Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.131890428A>C , CM000668.2:g.131890428A>C | GRCh38 |
| NC_000006.11:g.132211568A>C , CM000668.1:g.132211568A>C | GRCh37 |
| NC_000006.10:g.132253261A>C | NCBI36 |
| NG_008206.1:g.87413A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684674.1:n.1126A>C | ||
| ENST00000647893.1:c.2695A>C MANE Select | ENSP00000498074.1:p.Ser899Arg | |
| ENST00000360971.6:c.2695A>C | ENSP00000354238.2:p.Ser899Arg | |
| ENST00000513998.5:c.*1532A>C | ENSP00000422424.1:n.*1532A>C | |
| NM_006208.2:c.2695A>C | NP_006199.2:p.Ser899Arg | |
| XM_011535896.1:c.1585A>C | XP_011534198.1:p.Ser529Arg | |
| NM_006208.3:c.2695A>C MANE Select | NP_006199.2:p.Ser899Arg |