Linked Data
dbSNP Id:
rs1654207592
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.64832946G>C , CM000663.2:g.64832946G>C | GRCh38 |
| NC_000001.10:g.65298629G>C , CM000663.1:g.65298629G>C | GRCh37 |
| NC_000001.9:g.65071217G>C | NCBI36 |
| NG_023402.1:g.138559C>G | |
| NG_023402.2:g.239801C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000294428.8:c.*1961G>C MANE Select | ENSP00000294428.3:n.*1961G>C | |
| ENST00000294428.7:c.*1961G>C | ENSP00000294428.3:n.*1961G>C | |
| ENST00000371072.8:c.*1961G>C | ENSP00000360112.4:n.*1961G>C | |
| NM_018211.3:c.*1961G>C | NP_060681.2:n.*1961G>C | |
| XM_006710738.2:c.*1961G>C | XP_006710801.2:n.*1961G>C | |
| NM_001366165.1:c.*1961G>C | NP_001353094.1:n.*1961G>C | |
| XR_946693.3:n.4380G>C | ||
| NM_018211.4:c.*1961G>C | NP_060681.2:n.*1961G>C | |
| NM_001366165.2:c.*1961G>C MANE Select | NP_001353094.1:n.*1961G>C |