Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.16993206C>A , CM000670.2:g.16993206C>A | GRCh38 |
| NC_000008.10:g.16850715C>A , CM000670.1:g.16850715C>A | GRCh37 |
| NC_000008.9:g.16895086C>A | NCBI36 |
| NG_015978.1:g.13960G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000180166.6:c.502G>T MANE Select | ENSP00000180166.5:p.Ala168Ser | |
| ENST00000180166.5:c.502G>T | ENSP00000180166.5:p.Ala168Ser | |
| ENST00000519941.1:c.206G>T | ||
| NM_019851.2:c.502G>T | NP_062825.1:p.Ala168Ser | |
| NM_019851.3:c.502G>T MANE Select | NP_062825.1:p.Ala168Ser |