Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.155022487T>G , CM000685.2:g.155022487T>G | GRCh38 |
| NC_000023.10:g.154250762T>G , CM000685.1:g.154250762T>G | GRCh37 |
| NC_000023.9:g.153903956T>G | NCBI36 |
| NG_011403.1:g.5237A>C | |
| NG_011403.2:g.5237A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.66A>C MANE Select | ENSP00000353393.4:p.Arg22Ser | |
| ENST00000647125.1:c.66A>C | ENSP00000496062.1:p.Arg22Ser | |
| ENST00000360256.8:c.66A>C | ENSP00000353393.4:p.Arg22Ser | |
| ENST00000423959.5:c.38+4293A>C | ENSP00000409446.1:n.38+4293A>C | |
| ENST00000453950.1:c.48A>C | ENSP00000389153.1:p.Arg16Ser | |
| NM_000132.3:c.66A>C | NP_000123.1:p.Arg22Ser | |
| XM_011531126.1:c.38+4293A>C | XP_011529428.1:n.38+4293A>C | |
| NM_000132.4:c.66A>C MANE Select | NP_000123.1:p.Arg22Ser |