Linked Data
dbSNP Id:
rs2093760388
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2340828T>A , CM000678.2:g.2340828T>A | GRCh38 |
| NC_000016.9:g.2390829T>A , CM000678.1:g.2390829T>A | GRCh37 |
| NC_000016.8:g.2330830T>A | NCBI36 |
| NG_011790.1:g.4919A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000640929.1:n.42+1497T>A | ||
| ENST00000512848.5:n.182+1497T>A |