Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.3225646C>G , CM000668.2:g.3225646C>G | GRCh38 |
| NC_000006.11:g.3225880C>G , CM000668.1:g.3225880C>G | GRCh37 |
| NC_000006.10:g.3170879C>G | NCBI36 |
| NG_016715.1:g.7089G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000259818.8:c.443G>C MANE Select | ENSP00000259818.6:p.Gly148Ala | |
| ENST00000680070.1:n.1373G>C | ||
| ENST00000681707.1:n.1270G>C | ||
| ENST00000681757.1:n.748G>C | ||
| ENST00000259818.7:c.443G>C | ENSP00000259818.6:p.Gly148Ala | |
| ENST00000473006.1:n.560G>C | ||
| NM_178012.4:c.443G>C | NP_821080.1:p.Gly148Ala | |
| XM_011514571.1:c.227G>C | XP_011512873.1:p.Gly76Ala | |
| NM_178012.5:c.443G>C MANE Select | NP_821080.1:p.Gly148Ala |