Linked Data
dbSNP Id:
rs1577873816
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.67754530A>G , CM000666.2:g.67754530A>G | GRCh38 |
| NC_000004.11:g.68620248A>G , CM000666.1:g.68620248A>G | GRCh37 |
| NC_000004.10:g.68302843A>G | NCBI36 |
| NG_009293.1:g.6557T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NM_000406.2:c.-195T>C | NP_000397.1:n.-195T>C | |
| NM_001012763.1:c.-195T>C | NP_001012781.1:n.-195T>C |