Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.16993169C>T , CM000670.2:g.16993169C>T | GRCh38 |
| NC_000008.10:g.16850678C>T , CM000670.1:g.16850678C>T | GRCh37 |
| NC_000008.9:g.16895049C>T | NCBI36 |
| NG_015978.1:g.13997G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000180166.6:c.539G>A MANE Select | ENSP00000180166.5:p.Arg180Lys | |
| ENST00000180166.5:c.539G>A | ENSP00000180166.5:p.Arg180Lys | |
| ENST00000519941.1:c.243G>A | ||
| NM_019851.2:c.539G>A | NP_062825.1:p.Arg180Lys | |
| NM_019851.3:c.539G>A MANE Select | NP_062825.1:p.Arg180Lys |