Linked Data
dbSNP Id:
rs2121258887
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52814336T>C , CM000674.2:g.52814336T>C | GRCh38 |
| NC_000012.11:g.53208120T>C , CM000674.1:g.53208120T>C | GRCh37 |
| NC_000012.10:g.51494387T>C | NCBI36 |
| NG_007380.1:g.5216A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000551956.1:c.-278A>G | ENSP00000448220.1:n.-278A>G |