Linked Data
MyVariant Identifiers:
chr8:g.18257852C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.18400342C>G , CM000670.2:g.18400342C>G | GRCh38 |
| NC_000008.10:g.18257852C>G , CM000670.1:g.18257852C>G | GRCh37 |
| NC_000008.9:g.18302132C>G | NCBI36 |
| NG_012246.1:g.14098C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000286479.4:c.339C>G MANE Select | ENSP00000286479.3:p.Thr113= | |
| ENST00000286479.3:c.339C>G | ENSP00000286479.3:p.Thr113= | |
| ENST00000520116.1:c.-52C>G | ENSP00000428416.1:n.-52C>G | |
| NM_000015.2:c.339C>G | NP_000006.2:p.Thr113= | |
| XM_011544358.1:c.339C>G | XP_011542660.1:p.Thr113= | |
| XM_017012938.1:c.339C>G | XP_016868427.1:p.Thr113= | |
| NM_000015.3:c.339C>G MANE Select | NP_000006.2:p.Thr113= |