Linked Data
dbSNP Id:
rs1296871772
COSMIC:
COSM1453970
MyVariant Identifiers:
chr8:g.106814338C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.105802110C>T , CM000670.2:g.105802110C>T | GRCh38 |
| NC_000008.10:g.106814338C>T , CM000670.1:g.106814338C>T | GRCh37 |
| NC_000008.9:g.106883514C>T | NCBI36 |
| NG_011723.1:g.488192C>T | |
| NG_011723.2:g.488192C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000407775.7:c.2028C>T (ZFPM2) MANE Select | ENSP00000384179.2:p.Pro676= | |
| ENST00000407775.6:c.2028C>T (ZFPM2) | ENSP00000384179.2:p.Pro676= | |
| ENST00000517361.1:c.1632C>T (ZFPM2) | ENSP00000428720.1:p.Pro544= | |
| ENST00000520492.5:c.1632C>T (ZFPM2) | ENSP00000430757.1:p.Pro544= | |
| ENST00000522296.1:n.1822C>T (ZFPM2) | ||
| NM_012082.3:c.2028C>T (ZFPM2) | NP_036214.2:p.Pro676= | |
| NR_125796.1:n.180-3668G>A (ZFPM2-AS1) | ||
| NR_125797.1:n.191-3668G>A (ZFPM2-AS1) | ||
| XM_011516946.1:c.2067C>T (ZFPM2) | XP_011515248.1:p.Pro689= | |
| XM_011516947.1:c.1998C>T (ZFPM2) | XP_011515249.1:p.Pro666= | |
| XM_011516948.1:c.1869C>T (ZFPM2) | XP_011515250.1:p.Pro623= | |
| XM_011516949.1:c.1860C>T (ZFPM2) | XP_011515251.1:p.Pro620= | |
| NM_001362836.1:c.1869C>T (ZFPM2) | NP_001349765.1:p.Pro623= | |
| NM_001362837.1:c.1632C>T (ZFPM2) | NP_001349766.1:p.Pro544= | |
| XM_011516947.3:c.1998C>T (ZFPM2) | XP_011515249.1:p.Pro666= | |
| NM_012082.4:c.2028C>T (ZFPM2) MANE Select | NP_036214.2:p.Pro676= | |
| NM_001362836.2:c.1869C>T (ZFPM2) | NP_001349765.1:p.Pro623= | |
| NM_001362837.2:c.1632C>T (ZFPM2) | NP_001349766.1:p.Pro544= |