Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.136659363G>C , CM000685.2:g.136659363G>C | GRCh38 |
| NC_000023.10:g.135741522G>C , CM000685.1:g.135741522G>C | GRCh37 |
| NC_000023.9:g.135569188G>C | NCBI36 |
| NG_007280.1:g.16187G>C , LRG_141:g.16187G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695724.1:c.*352G>C | ENSP00000512122.1:n.*352G>C | |
| ENST00000695725.1:c.*289G>C | ENSP00000512123.1:n.*289G>C | |
| ENST00000695726.1:n.2702G>C | ||
| ENST00000695729.1:n.3537G>C | ||
| ENST00000370629.7:c.734G>C MANE Select | ENSP00000359663.2:p.Ser245Thr | |
| ENST00000370628.2:c.671G>C | ENSP00000359662.2:p.Ser224Thr | |
| ENST00000370629.6:c.734G>C | ENSP00000359663.2:p.Ser245Thr | |
| NM_000074.2:c.734G>C , LRG_141t1:c.734G>C | NP_000065.1:p.Ser245Thr | |
| NM_000074.3:c.734G>C MANE Select | NP_000065.1:p.Ser245Thr |