Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.136046389C>A , CM000667.2:g.136046389C>A | GRCh38 |
| NC_000005.9:g.135382078C>A , CM000667.1:g.135382078C>A | GRCh37 |
| NC_000005.8:g.135409977C>A | NCBI36 |
| NG_012646.1:g.22495C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000442011.7:c.353C>A MANE Select | ENSP00000416330.2:p.Thr118Asn | |
| ENST00000442011.6:c.353C>A | ENSP00000416330.2:p.Thr118Asn | |
| ENST00000504185.5:n.510C>A | ||
| ENST00000506699.5:n.418C>A | ||
| ENST00000507018.5:c.270C>A | ||
| ENST00000515433.1:n.645C>A | ||
| NM_000358.2:c.353C>A | NP_000349.1:p.Thr118Asn | |
| NM_000358.3:c.353C>A MANE Select | NP_000349.1:p.Thr118Asn |