Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.95324422C>G , CM000669.2:g.95324422C>G | GRCh38 |
| NC_000007.13:g.94953734C>G , CM000669.1:g.94953734C>G | GRCh37 |
| NC_000007.12:g.94791670C>G | NCBI36 |
| NG_008779.1:g.5151G>C | |
| NG_008779.2:g.5285G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222381.8:c.54G>C MANE Select | ENSP00000222381.3:p.Arg18Ser | |
| ENST00000222381.7:c.54G>C | ENSP00000222381.3:p.Arg18Ser | |
| ENST00000433729.1:c.54G>C | ENSP00000407359.1:p.Arg18Ser | |
| NM_000446.5:c.54G>C | NP_000437.3:p.Arg18Ser | |
| NM_000446.6:c.54G>C | NP_000437.3:p.Arg18Ser | |
| NM_000446.7:c.54G>C MANE Select | NP_000437.3:p.Arg18Ser |