Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.47733888T>C , CM000679.2:g.47733888T>C | GRCh38 |
| NC_000017.10:g.45811254T>C , CM000679.1:g.45811254T>C | GRCh37 |
| NC_000017.9:g.43166253T>C | NCBI36 |
| NG_012166.1:g.5645T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000177694.2:c.434T>C MANE Select | ENSP00000177694.1:p.Leu145Pro | |
| ENST00000177694.1:c.434T>C | ENSP00000177694.1:p.Leu145Pro | |
| ENST00000581328.1:n.464T>C | ||
| NM_013351.1:c.434T>C | NP_037483.1:p.Leu145Pro | |
| XM_011524698.1:c.434T>C | XP_011523000.1:p.Leu145Pro | |
| NM_013351.2:c.434T>C MANE Select | NP_037483.1:p.Leu145Pro |