Linked Data
ClinVar Variation Id:
1706101
ClinVar RCV Id:
RCV002284631
dbSNP Id:
rs2135832748
COSMIC:
COSM1209834
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.120988964C>A , CM000674.2:g.120988964C>A | GRCh38 |
| NC_000012.11:g.121426767C>A , CM000674.1:g.121426767C>A | GRCh37 |
| NC_000012.10:g.119911150C>A | NCBI36 |
| NG_011731.2:g.15219C>A , LRG_522:g.15219C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000560968.6:c.458C>A | ENSP00000453965.2:p.Pro153His | |
| ENST00000257555.11:c.458C>A MANE Select | ENSP00000257555.5:p.Pro153His | |
| ENST00000257555.10:c.458C>A | ENSP00000257555.4:p.Pro153His | |
| ENST00000400024.6:c.458C>A | ENSP00000476181.1:p.Pro153His | |
| ENST00000402929.5:n.593C>A | ||
| ENST00000535955.5:n.43-8527C>A | ||
| ENST00000538626.2:n.191-8527C>A | ||
| ENST00000538646.5:c.458C>A | ENSP00000443964.1:p.Pro153His | |
| ENST00000540108.1:c.327-4556C>A | ENSP00000445445.1:n.327-4556C>A | |
| ENST00000541395.5:c.458C>A | ENSP00000443112.1:p.Pro153His | |
| ENST00000541924.5:c.458C>A | ENSP00000440361.1:p.Pro153His | |
| ENST00000543427.5:c.458C>A | ENSP00000439721.2:p.Pro153His | |
| ENST00000544413.2:c.458C>A | ENSP00000438804.1:p.Pro153His | |
| ENST00000544574.5:c.73-7653C>A | ENSP00000438565.1:n.73-7653C>A | |
| ENST00000560968.5:c.601C>A | ||
| ENST00000615446.4:c.-257-7298C>A | ENSP00000483994.1:n.-257-7298C>A | |
| ENST00000617366.4:c.458C>A | ENSP00000481967.1:p.Pro153His | |
| NM_000545.5:c.458C>A , LRG_522t1:c.458C>A | NP_000536.5:p.Pro153His | |
| NM_000545.6:c.458C>A | NP_000536.5:p.Pro153His | |
| NM_001306179.1:c.458C>A | NP_001293108.1:p.Pro153His | |
| XM_005253931.2:c.458C>A | XP_005253988.1:p.Pro153His | |
| XM_024449168.1:c.458C>A | XP_024304936.1:p.Pro153His | |
| NM_000545.8:c.458C>A MANE Select | NP_000536.6:p.Pro153His | |
| NM_001306179.2:c.458C>A | NP_001293108.2:p.Pro153His |