Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.178981486T>C , CM000667.2:g.178981486T>C | GRCh38 |
| NC_000005.9:g.178408487T>C , CM000667.1:g.178408487T>C | GRCh37 |
| NC_000005.8:g.178341093T>C | NCBI36 |
| NG_008105.1:g.18638A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000517717.3:c.*171A>G MANE Select | ENSP00000430767.1:n.*171A>G | |
| ENST00000650031.1:c.*171A>G | ENSP00000497110.1:n.*171A>G | |
| ENST00000650488.1:n.1528A>G | ||
| ENST00000231188.9:c.*171A>G | ENSP00000231188.5:n.*171A>G | |
| NM_000843.3:c.*171A>G | NP_000834.2:n.*171A>G | |
| XR_941310.1:n.1470-8261T>C | ||
| NM_000843.4:c.*171A>G MANE Select | NP_000834.2:n.*171A>G |