Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153690405C>G , CM000685.2:g.153690405C>G | GRCh38 |
| NC_000023.10:g.152955860C>G , CM000685.1:g.152955860C>G | GRCh37 |
| NC_000023.9:g.152609054C>G | NCBI36 |
| NG_012016.1:g.7109C>G | |
| NG_012016.2:g.7109C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253122.10:c.293C>G MANE Select | ENSP00000253122.5:p.Ala98Gly | |
| ENST00000675713.1:n.47C>G | ||
| ENST00000253122.9:c.293C>G | ENSP00000253122.5:p.Ala98Gly | |
| ENST00000430077.6:c.-53C>G | ENSP00000403041.2:n.-53C>G | |
| ENST00000476466.1:n.145C>G | ||
| NM_001142805.1:c.293C>G | NP_001136277.1:p.Ala98Gly | |
| NM_001142806.1:c.-53C>G | NP_001136278.1:n.-53C>G | |
| NM_005629.3:c.293C>G | NP_005620.1:p.Ala98Gly | |
| NM_005629.4:c.293C>G MANE Select | NP_005620.1:p.Ala98Gly | |
| NM_001142805.2:c.293C>G | NP_001136277.1:p.Ala98Gly |