Linked Data
dbSNP Id:
rs2072165585
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.122050488T>C , CM000665.2:g.122050488T>C | GRCh38 |
| NC_000003.11:g.121769335T>C , CM000665.1:g.121769335T>C | GRCh37 |
| NC_000003.10:g.123252025T>C | NCBI36 |
| NG_029928.1:g.127T>C | |
| NG_031870.2:g.15067A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011512739.1:c.-348+9932A>G | XP_011511041.1:n.-348+9932A>G | |
| XM_011512739.2:c.-348+9932A>G | XP_011511041.1:n.-348+9932A>G |