Linked Data
dbSNP Id:
rs1156546702
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.87123989T>A , CM000665.2:g.87123989T>A | GRCh38 |
| NC_000003.11:g.87173139T>A , CM000665.1:g.87173139T>A | GRCh37 |
| NC_000003.10:g.87255829T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_104153.1:n.329-30349T>A |