Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.114045258A>C , CM000672.2:g.114045258A>C | GRCh38 |
| NC_000010.10:g.115805017A>C , CM000672.1:g.115805017A>C | GRCh37 |
| NC_000010.9:g.115795007A>C | NCBI36 |
| NG_012187.1:g.6212A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369295.4:c.1126A>C MANE Select | ENSP00000358301.2:p.Ile376Leu | |
| ENST00000369295.3:c.1126A>C | ENSP00000358301.2:p.Ile376Leu | |
| NM_000684.2:c.1126A>C | NP_000675.1:p.Ile376Leu | |
| NM_000684.3:c.1126A>C MANE Select | NP_000675.1:p.Ile376Leu |