Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.206116706A>G , CM000663.2:g.206116706A>G | GRCh38 |
| NC_000001.10:g.206224625T>C , CM000663.1:g.206224625T>C | GRCh37 |
| NC_000001.9:g.204391248T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000367126.5:c.185T>C MANE Select | ENSP00000356094.4:p.Leu62Pro | |
| ENST00000367126.4:c.185T>C | ENSP00000356094.4:p.Leu62Pro | |
| ENST00000612906.1:n.36+958T>C | ||
| NM_000707.3:c.185T>C | NP_000698.1:p.Leu62Pro | |
| NM_000707.4:c.185T>C | NP_000698.1:p.Leu62Pro | |
| NM_000707.5:c.185T>C MANE Select | NP_000698.1:p.Leu62Pro |