Linked Data
dbSNP Id:
rs1791760176
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94404750A>G , CM000669.2:g.94404750A>G | GRCh38 |
| NC_000007.13:g.94034062A>G , CM000669.1:g.94034062A>G | GRCh37 |
| NC_000007.12:g.93871998A>G | NCBI36 |
| NG_007405.1:g.15190A>G , LRG_2:g.15190A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297268.11:c.378+4A>G MANE Select | ENSP00000297268.6:n.378+4A>G | |
| ENST00000297268.10:c.378+4A>G | ENSP00000297268.6:n.378+4A>G | |
| ENST00000620463.1:c.372+4A>G | ENSP00000477719.1:n.372+4A>G | |
| NM_000089.3:c.378+4A>G , LRG_2t1:c.378+4A>G | NP_000080.2:n.378+4A>G | |
| NM_000089.4:c.378+4A>G MANE Select | NP_000080.2:n.378+4A>G |