Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.55154111C>G , CM000681.2:g.55154111C>G | GRCh38 |
| NC_000019.9:g.55665479C>G , CM000681.1:g.55665479C>G | GRCh37 |
| NC_000019.8:g.60357291C>G | NCBI36 |
| NG_007866.2:g.8622G>C , LRG_432:g.8622G>C | |
| NG_011829.2:g.128G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344887.10:c.468G>C MANE Select | ENSP00000341838.5:p.Gln156His | |
| ENST00000665070.1:c.501G>C | ENSP00000499482.1:p.Gln167His | |
| ENST00000344887.9:c.468G>C | ENSP00000341838.5:p.Gln156His | |
| ENST00000585806.5:n.467G>C | ||
| ENST00000586669.5:n.476G>C | ||
| ENST00000588882.1:c.393G>C | ENSP00000466729.1:p.Gln131His | |
| ENST00000589864.1:n.296G>C | ||
| NM_000363.4:c.468G>C , LRG_432t1:c.468G>C | NP_000354.4:p.Gln156His | |
| NM_000363.5:c.468G>C MANE Select | NP_000354.4:p.Gln156His |