Linked Data
dbSNP Id:
rs2133558735
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.2444927C>G , CM000673.2:g.2444927C>G | GRCh38 |
| NC_000011.9:g.2466157C>G , CM000673.1:g.2466157C>G | GRCh37 |
| NC_000011.8:g.2422733C>G | NCBI36 |
| NG_008935.1:g.4937C>G , LRG_287:g.4937C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000496887.7:c.23+219C>G | ENSP00000434560.2:n.23+219C>G | |
| ENST00000496887.6:c.23+219C>G | ENSP00000434560.1:n.23+219C>G |