Linked Data
dbSNP Id:
rs2092606403
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.149928300T>G , CM000663.2:g.149928300T>G | GRCh38 |
| NC_000001.10:g.149900192T>G , CM000663.1:g.149900192T>G | GRCh37 |
| NC_000001.9:g.148166816T>G | NCBI36 |
| NG_032777.1:g.4953A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271628.8:c.-541A>C | ENSP00000271628.8:n.-541A>C |