Linked Data
dbSNP Id:
rs1589019501
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.62610277G>C , CM000672.2:g.62610277G>C | GRCh38 |
| NC_000010.10:g.64370036G>C , CM000672.1:g.64370036G>C | GRCh37 |
| NC_000010.9:g.64040042G>C | NCBI36 |
| NG_021209.1:g.241121G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000647733.1:c.982-12826G>C | ENSP00000502188.1:n.982-12826G>C | |
| ENST00000395251.5:c.-184-33465G>C | ENSP00000378672.1:n.-184-33465G>C | |
| ENST00000410046.7:c.982-12826G>C | ENSP00000387091.3:n.982-12826G>C | |
| NM_199451.2:c.982-12826G>C | NP_955523.1:n.982-12826G>C | |
| NM_199452.3:c.-184-33465G>C | NP_955524.3:n.-184-33465G>C | |
| NM_199451.3:c.982-12826G>C | NP_955523.1:n.982-12826G>C |