Linked Data
ClinVar Variation Id:
2029985
ClinVar RCV Id:
RCV002881094
dbSNP Id:
rs2100940850
MyVariant Identifiers:
chr1:g.11308095G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.11248038G>A , CM000663.2:g.11248038G>A | GRCh38 |
| NC_000001.10:g.11308095G>A , CM000663.1:g.11308095G>A | GRCh37 |
| NC_000001.9:g.11230682G>A | NCBI36 |
| NG_033239.1:g.19514C>T , LRG_734:g.19514C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703118.1:c.897C>T | ENSP00000515181.1:p.Tyr299= | |
| ENST00000703132.1:n.878C>T | ||
| ENST00000703140.1:c.897C>T | ENSP00000515197.1:p.Tyr299= | |
| ENST00000703141.1:c.897C>T | ENSP00000515198.1:p.Tyr299= | |
| ENST00000703142.1:c.897C>T | ENSP00000515199.1:p.Tyr299= | |
| ENST00000703143.1:c.897C>T | ENSP00000515200.1:p.Tyr299= | |
| ENST00000361445.9:c.897C>T MANE Select | ENSP00000354558.4:p.Tyr299= | |
| ENST00000361445.8:c.897C>T | ENSP00000354558.4:p.Tyr299= | |
| NM_004958.3:c.897C>T , LRG_734t1:c.897C>T | NP_004949.1:p.Tyr299= | |
| XM_005263438.1:c.897C>T | XP_005263495.1:p.Tyr299= | |
| XM_011541166.1:c.897C>T | XP_011539468.1:p.Tyr299= | |
| XR_244786.1:n.1018C>T | ||
| XM_005263438.2:c.897C>T | XP_005263495.1:p.Tyr299= | |
| XM_011541166.2:c.897C>T | XP_011539468.1:p.Tyr299= | |
| XM_017000900.1:c.216C>T | XP_016856389.1:p.Tyr72= | |
| XM_017000901.1:c.-243C>T | XP_016856390.1:n.-243C>T | |
| XM_017000902.1:c.897C>T | XP_016856391.1:p.Tyr299= | |
| XM_024446187.1:c.897C>T | XP_024301955.1:p.Tyr299= | |
| XR_001737087.1:n.1018C>T | ||
| NM_004958.4:c.897C>T MANE Select | NP_004949.1:p.Tyr299= | |
| NM_001386500.1:c.897C>T | NP_001373429.1:p.Tyr299= | |
| NM_001386501.1:c.-243C>T | NP_001373430.1:n.-243C>T |