Linked Data
dbSNP Id:
rs2138916656
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.109767099T>C , CM000675.2:g.109767099T>C | GRCh38 |
| NC_000013.10:g.110419446T>C , CM000675.1:g.110419446T>C | GRCh37 |
| NC_000013.9:g.109217447T>C | NCBI36 |
| NG_008154.1:g.24469A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375856.5:c.4013-10791A>G MANE Select | ENSP00000365016.3:n.4013-10791A>G | |
| ENST00000375856.4:c.4013-10791A>G | ENSP00000365016.3:n.4013-10791A>G | |
| NM_003749.2:c.4013-10791A>G | NP_003740.2:n.4013-10791A>G | |
| NM_003749.3:c.4013-10791A>G MANE Select | NP_003740.2:n.4013-10791A>G |