Linked Data
dbSNP Id:
rs1755650848
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.119320651T>C , CM000666.2:g.119320651T>C | GRCh38 |
| NC_000004.11:g.120241806T>C , CM000666.1:g.120241806T>C | GRCh37 |
| NC_000004.10:g.120461254T>C | NCBI36 |
| NG_011444.1:g.6511A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000274024.4:c.240+19A>G MANE Select | ENSP00000274024.3:n.240+19A>G | |
| ENST00000274024.3:c.240+19A>G | ENSP00000274024.3:n.240+19A>G | |
| NM_000134.3:c.240+19A>G | NP_000125.2:n.240+19A>G | |
| NM_000134.4:c.240+19A>G MANE Select | NP_000125.2:n.240+19A>G |