Linked Data
ClinVar Variation Id:
2964498
ClinVar RCV Id:
RCV003820600
dbSNP Id:
rs1876938904
gnomAD v4:
12-120993691-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.120993691T>C , CM000674.2:g.120993691T>C | GRCh38 |
| NC_000012.11:g.121431494T>C , CM000674.1:g.121431494T>C | GRCh37 |
| NC_000012.10:g.119915877T>C | NCBI36 |
| NG_011731.2:g.19946T>C , LRG_522:g.19946T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000560968.6:c.698T>C | ENSP00000453965.2:p.Val233Ala | |
| ENST00000257555.11:c.698T>C MANE Select | ENSP00000257555.5:p.Val233Ala | |
| ENST00000257555.10:c.698T>C | ENSP00000257555.4:p.Val233Ala | |
| ENST00000400024.6:c.698T>C | ENSP00000476181.1:p.Val233Ala | |
| ENST00000402929.5:n.833T>C | ||
| ENST00000535955.5:n.43-3800T>C | ||
| ENST00000538626.2:n.191-3800T>C | ||
| ENST00000538646.5:c.527-473T>C | ENSP00000443964.1:n.527-473T>C | |
| ENST00000540108.1:c.*138T>C | ENSP00000445445.1:n.*138T>C | |
| ENST00000541395.5:c.698T>C | ENSP00000443112.1:p.Val233Ala | |
| ENST00000541924.5:c.698T>C | ENSP00000440361.1:p.Val233Ala | |
| ENST00000543427.5:c.633+65T>C | ENSP00000439721.2:n.633+65T>C | |
| ENST00000544413.2:c.698T>C | ENSP00000438804.1:p.Val233Ala | |
| ENST00000544574.5:c.73-2926T>C | ENSP00000438565.1:n.73-2926T>C | |
| ENST00000560968.5:c.841T>C | ||
| ENST00000615446.4:c.-257-2571T>C | ENSP00000483994.1:n.-257-2571T>C | |
| ENST00000617366.4:c.586+112T>C | ENSP00000481967.1:n.586+112T>C | |
| NM_000545.5:c.698T>C , LRG_522t1:c.698T>C | NP_000536.5:p.Val233Ala | |
| NM_000545.6:c.698T>C | NP_000536.5:p.Val233Ala | |
| NM_001306179.1:c.698T>C | NP_001293108.1:p.Val233Ala | |
| XM_005253931.2:c.698T>C | XP_005253988.1:p.Val233Ala | |
| XM_024449168.1:c.698T>C | XP_024304936.1:p.Val233Ala | |
| NM_000545.8:c.698T>C MANE Select | NP_000536.6:p.Val233Ala | |
| NM_001306179.2:c.698T>C | NP_001293108.2:p.Val233Ala |