Linked Data
MyVariant Identifiers:
chr9:g.35657941A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.35657944A>G , CM000671.2:g.35657944A>G | GRCh38 |
| NC_000009.11:g.35657941A>G , CM000671.1:g.35657941A>G | GRCh37 |
| NC_000009.10:g.35647941A>G | NCBI36 |
| NG_017041.1:g.5075T>C , LRG_163:g.5075T>C | |
| NG_033120.1:g.4655A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_003051.3:n.75T>C , LRG_163t1:n.75T>C |