Linked Data
dbSNP Id:
rs2092284944
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.149884423G>C , CM000663.2:g.149884423G>C | GRCh38 |
| NC_000001.10:g.149855973G>C , CM000663.1:g.149855973G>C | GRCh37 |
| NC_000001.9:g.148122597G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369160.3:c.377+1841C>G | ENSP00000375736.2:n.377+1841C>G |