Linked Data
dbSNP Id:
rs2088840096
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.28835000T>C , CM000663.2:g.28835000T>C | GRCh38 |
| NC_000001.10:g.29161512T>C , CM000663.1:g.29161512T>C | GRCh37 |
| NC_000001.9:g.29034099T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000234961.7:c.227+22390T>C MANE Select | ENSP00000234961.2:n.227+22390T>C | |
| ENST00000234961.6:c.227+22390T>C | ENSP00000234961.2:n.227+22390T>C | |
| ENST00000621425.1:c.227+22390T>C | ENSP00000477970.1:n.227+22390T>C | |
| NM_000911.3:c.227+22390T>C | NP_000902.3:n.227+22390T>C | |
| NM_000911.4:c.227+22390T>C MANE Select | NP_000902.3:n.227+22390T>C |