Linked Data
dbSNP Id:
rs2077748170
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108147607T>A , CM000673.2:g.108147607T>A | GRCh38 |
| NC_000011.9:g.108018334T>A , CM000673.1:g.108018334T>A | GRCh37 |
| NC_000011.8:g.107523544T>A | NCBI36 |
| NG_009888.1:g.31077T>A | |
| NG_009888.2:g.35903T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265838.8:c.*217T>A | ENSP00000265838.4:n.*217T>A | |
| NM_000019.3:c.*217T>A | NP_000010.1:n.*217T>A | |
| XM_006718834.2:c.*217T>A | XP_006718897.1:n.*217T>A | |
| XM_006718835.2:c.*217T>A | XP_006718898.1:n.*217T>A | |
| XM_017017682.2:c.*217T>A | XP_016873171.1:n.*217T>A | |
| XM_017017683.2:c.*217T>A | XP_016873172.1:n.*217T>A |