Linked Data
dbSNP Id:
rs1052667
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.47004177C>G , CM000681.2:g.47004177C>G | GRCh38 |
| NC_000019.9:g.47507434C>G , CM000681.1:g.47507434C>G | GRCh37 |
| NC_000019.8:g.52199274C>G | NCBI36 |
| NG_047014.1:g.90611C>G | |
| NG_047014.2:g.148181C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000404338.8:c.7989C>G | ENSP00000385720.2:n.7989C>G | |
| ENST00000672722.1:c.*3489C>G MANE Select | ENSP00000500409.1:n.*3489C>G | |
| ENST00000404338.7:c.7989C>G | ENSP00000385720.2:n.7989C>G | |
| ENST00000614079.1:c.7566C>G | ENSP00000483730.1:n.7566C>G | |
| NM_004491.4:c.7989C>G | NP_004482.4:n.7989C>G | |
| NM_004491.5:c.*3489C>G MANE Select | NP_004482.4:n.*3489C>G |