Linked Data
dbSNP Id:
rs2101741794
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.114713824G>T , CM000663.2:g.114713824G>T | GRCh38 |
| NC_000001.10:g.115256445G>T , CM000663.1:g.115256445G>T | GRCh37 |
| NC_000001.9:g.115057968G>T | NCBI36 |
| NG_007572.1:g.8071C>A , LRG_92:g.8071C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369535.5:c.266C>A MANE Select | ENSP00000358548.4:p.Ser89Ter | |
| ENST00000369535.4:c.266C>A | ENSP00000358548.4:p.Ser89Ter | |
| NM_002524.4:c.266C>A | NP_002515.1:p.Ser89Ter | |
| NM_002524.5:c.266C>A MANE Select | NP_002515.1:p.Ser89Ter |