Linked Data
dbSNP Id:
rs1236169290
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.68737247C>G , CM000678.2:g.68737247C>G | GRCh38 |
| NC_000016.9:g.68771150C>G , CM000678.1:g.68771150C>G | GRCh37 |
| NC_000016.8:g.67328651C>G | NCBI36 |
| NG_008021.1:g.4956C>G , LRG_301:g.4956C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261769.9:c.-169C>G | ENSP00000261769.4:n.-169C>G |