Linked Data
ClinVar Variation Id:
1087076
ClinVar RCV Id:
RCV001405040
dbSNP Id:
rs777132315
ExAC:
1:11217316 G / A
gnomAD v2:
1-11217316-G-A
gnomAD v4:
1-11157259-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.11157259G>A , CM000663.2:g.11157259G>A | GRCh38 |
| NC_000001.10:g.11217316G>A , CM000663.1:g.11217316G>A | GRCh37 |
| NC_000001.9:g.11139903G>A | NCBI36 |
| NG_033239.1:g.110293C>T , LRG_734:g.110293C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703118.1:c.4362C>T | ENSP00000515181.1:p.His1454= | |
| ENST00000703131.1:n.282C>T | ||
| ENST00000703140.1:c.4149C>T | ENSP00000515197.1:p.His1383= | |
| ENST00000703141.1:c.4362C>T | ENSP00000515198.1:p.His1454= | |
| ENST00000703142.1:c.*1192C>T | ENSP00000515199.1:n.*1192C>T | |
| ENST00000361445.9:c.4362C>T MANE Select | ENSP00000354558.4:p.His1454= | |
| ENST00000361445.8:c.4362C>T | ENSP00000354558.4:p.His1454= | |
| NM_004958.3:c.4362C>T , LRG_734t1:c.4362C>T | NP_004949.1:p.His1454= | |
| XM_005263438.1:c.4362C>T | XP_005263495.1:p.His1454= | |
| XM_011541166.1:c.4362C>T | XP_011539468.1:p.His1454= | |
| XR_244786.1:n.4483C>T | ||
| XM_005263438.2:c.4362C>T | XP_005263495.1:p.His1454= | |
| XM_011541166.2:c.4362C>T | XP_011539468.1:p.His1454= | |
| XM_017000900.1:c.3681C>T | XP_016856389.1:p.His1227= | |
| XM_017000901.1:c.3114C>T | XP_016856390.1:p.His1038= | |
| XM_024446187.1:c.4362C>T | XP_024301955.1:p.His1454= | |
| XR_001737087.1:n.4483C>T | ||
| NM_004958.4:c.4362C>T MANE Select | NP_004949.1:p.His1454= | |
| NM_001386500.1:c.4362C>T | NP_001373429.1:p.His1454= | |
| NM_001386501.1:c.3114C>T | NP_001373430.1:p.His1038= |