Linked Data
dbSNP Id:
rs1686630298
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.113117821C>G , CM000664.2:g.113117821C>G | GRCh38 |
| NC_000002.11:g.113875398C>G , CM000664.1:g.113875398C>G | GRCh37 |
| NC_000002.10:g.113591869C>G | NCBI36 |
| NG_021240.1:g.4929C>G , LRG_188:g.4929C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000409052.6:c.-272-2245C>G | ENSP00000387210.1:n.-272-2245C>G | |
| ENST00000465812.6:n.775+156C>G | ||
| ENST00000409052.5:c.-272-2245C>G | ENSP00000387210.1:n.-272-2245C>G | |
| XM_011511121.1:c.-272-2245C>G | XP_011509423.1:n.-272-2245C>G |