Linked Data
MyVariant Identifiers:
chr9:g.35657934T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.35657937T>G , CM000671.2:g.35657937T>G | GRCh38 |
| NC_000009.11:g.35657934T>G , CM000671.1:g.35657934T>G | GRCh37 |
| NC_000009.10:g.35647934T>G | NCBI36 |
| NG_017041.1:g.5082A>C , LRG_163:g.5082A>C | |
| NG_033120.1:g.4648T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_003051.3:n.82A>C , LRG_163t1:n.82A>C |