Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.31820149G>C , CM000682.2:g.31820149G>C | GRCh38 |
| NC_000020.10:g.30407952G>C , CM000682.1:g.30407952G>C | GRCh37 |
| NC_000020.9:g.29871613G>C | NCBI36 |
| NG_012847.1:g.5775G>C , LRG_392:g.5775G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375985.5:c.76G>C MANE Select | ENSP00000365152.4:p.Gly26Arg | |
| ENST00000375985.4:c.76G>C | ENSP00000365152.4:p.Gly26Arg | |
| ENST00000375994.6:c.76G>C | ENSP00000365162.2:p.Gly26Arg | |
| NM_033118.3:c.76G>C , LRG_392t1:c.76G>C | NP_149109.1:p.Gly26Arg | |
| XR_244155.1:n.241G>C | ||
| NM_033118.4:c.76G>C MANE Select | NP_149109.1:p.Gly26Arg |