Linked Data
dbSNP Id:
rs1877600138
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.121846825A>G , CM000674.2:g.121846825A>G | GRCh38 |
| NC_000012.11:g.122284731A>G , CM000674.1:g.122284731A>G | GRCh37 |
| NC_000012.10:g.120769114A>G | NCBI36 |
| NG_016461.1:g.46787T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000289004.8:c.831+37T>C MANE Select | ENSP00000289004.4:n.831+37T>C | |
| ENST00000543163.5:c.714+37T>C | ENSP00000441677.1:n.714+37T>C | |
| NM_001171993.1:c.714+37T>C | NP_001165464.1:n.714+37T>C | |
| NM_002150.2:c.831+37T>C | NP_002141.1:n.831+37T>C | |
| NM_002150.3:c.831+37T>C MANE Select | NP_002141.2:n.831+37T>C | |
| NM_001171993.2:c.714+37T>C | NP_001165464.1:n.714+37T>C |