Linked Data
dbSNP Id:
rs2070097453
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19967204C>T , CM000670.2:g.19967204C>T | GRCh38 |
| NC_000008.10:g.19824715C>T , CM000670.1:g.19824715C>T | GRCh37 |
| NC_000008.9:g.19868995C>T | NCBI36 |
| NG_008855.1:g.33134C>T | |
| NG_008855.2:g.70488C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650287.1:c.*1894C>T MANE Select | ENSP00000497642.1:n.*1894C>T | |
| ENST00000311322.8:c.*1894C>T | ENSP00000309757.6:n.*1894C>T | |
| NM_000237.2:c.*1894C>T | NP_000228.1:n.*1894C>T | |
| NM_000237.3:c.*1894C>T MANE Select | NP_000228.1:n.*1894C>T |