Linked Data
dbSNP Id:
rs1806599006
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.6877998A>G , CM000670.2:g.6877998A>G | GRCh38 |
| NC_000008.10:g.6735520A>G , CM000670.1:g.6735520A>G | GRCh37 |
| NC_000008.9:g.6722930A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297439.3:c.-141T>C | ENSP00000297439.3:n.-141T>C | |
| NM_005218.3:c.-141T>C | NP_005209.1:n.-141T>C |