Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.136659051C>G , CM000685.2:g.136659051C>G | GRCh38 |
| NC_000023.10:g.135741210C>G , CM000685.1:g.135741210C>G | GRCh37 |
| NC_000023.9:g.135568876C>G | NCBI36 |
| NG_007280.1:g.15875C>G , LRG_141:g.15875C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695724.1:c.*40C>G | ENSP00000512122.1:n.*40C>G | |
| ENST00000695725.1:c.169C>G | ENSP00000512123.1:p.Leu57Val | |
| ENST00000695726.1:n.2390C>G | ||
| ENST00000695729.1:n.3225C>G | ||
| ENST00000370629.7:c.422C>G MANE Select | ENSP00000359663.2:p.Ala141Gly | |
| ENST00000370628.2:c.359C>G | ENSP00000359662.2:p.Ala120Gly | |
| ENST00000370629.6:c.422C>G | ENSP00000359663.2:p.Ala141Gly | |
| NM_000074.2:c.422C>G , LRG_141t1:c.422C>G | NP_000065.1:p.Ala141Gly | |
| NM_000074.3:c.422C>G MANE Select | NP_000065.1:p.Ala141Gly |