Linked Data
dbSNP Id:
rs2150951481
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32636647C>T , CM000668.2:g.32636647C>T | GRCh38 |
| NC_000006.11:g.32604424C>T , CM000668.1:g.32604424C>T | GRCh37 |
| NC_000006.10:g.32712402C>T | NCBI36 |
| NG_032876.1:g.4242C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000422863.1:c.-38-774C>T | ENSP00000405797.1:n.-38-774C>T |