Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.47572934C>G , CM000685.2:g.47572934C>G | GRCh38 |
| NC_000023.10:g.47432333C>G , CM000685.1:g.47432333C>G | GRCh37 |
| NC_000023.9:g.47317277C>G | NCBI36 |
| NG_008437.1:g.51924G>C | |
| NG_016339.1:g.16818C>G | |
| NG_016339.2:g.16818C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295987.13:c.2048G>C MANE Select | ENSP00000295987.7:p.Ser683Thr | |
| ENST00000340666.5:c.2010G>C | ENSP00000343206.4:p.Ter670Tyr | |
| ENST00000640721.1:c.98G>C | ENSP00000492857.1:p.Ser33Thr | |
| ENST00000295987.11:c.2048G>C | ENSP00000295987.7:p.Ser683Thr | |
| ENST00000340666.4:c.2010G>C | ENSP00000343206.4:p.Ter670Tyr | |
| NM_006950.3:c.2048G>C MANE Select | NP_008881.2:p.Ser683Thr | |
| NM_133499.2:c.2010G>C | NP_598006.1:p.Ter670Tyr |