Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6714073C>G , CM000681.2:g.6714073C>G | GRCh38 |
| NC_000019.9:g.6714084C>G , CM000681.1:g.6714084C>G | GRCh37 |
| NC_000019.8:g.6665084C>G | NCBI36 |
| NG_009557.1:g.11579G>C , LRG_27:g.11579G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695652.1:c.569G>C | ENSP00000512083.1:p.Ser190Thr | |
| ENST00000245907.11:c.692G>C MANE Select | ENSP00000245907.4:p.Ser231Thr | |
| ENST00000245907.10:c.692G>C | ENSP00000245907.4:p.Ser231Thr | |
| ENST00000595577.1:n.196G>C | ||
| NM_000064.3:c.692G>C | NP_000055.2:p.Ser231Thr | |
| NM_000064.4:c.692G>C MANE Select | NP_000055.2:p.Ser231Thr |