Linked Data
dbSNP Id:
rs2073151208
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.17265141C>T , CM000663.2:g.17265141C>T | GRCh38 |
| NC_000001.10:g.17591636C>T , CM000663.1:g.17591636C>T | GRCh37 |
| NC_000001.9:g.17464223C>T | NCBI36 |
| NG_052788.1:g.21063C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375460.3:c.347-518C>T MANE Select | ENSP00000364609.3:n.347-518C>T | |
| NM_016233.2:c.347-518C>T MANE Select | NP_057317.2:n.347-518C>T | |
| XM_006710684.2:c.233-518C>T | XP_006710747.1:n.233-518C>T | |
| XM_011541571.1:c.233-518C>T | XP_011539873.1:n.233-518C>T | |
| XM_011541572.1:c.347-518C>T | XP_011539874.1:n.347-518C>T | |
| XM_011541571.2:c.233-518C>T | XP_011539873.1:n.233-518C>T | |
| XM_011541572.2:c.347-518C>T | XP_011539874.1:n.347-518C>T |