Linked Data
ClinVar Variation Id:
138136
dbSNP Id:
rs199830303
ExAC:
18:2921658 T / A
gnomAD v2:
18-2921658-T-A
gnomAD v3:
18-2921660-T-A
gnomAD v4:
18-2921660-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.2921660T>A , CM000680.2:g.2921660T>A | GRCh38 |
| NC_000018.9:g.2921658T>A , CM000680.1:g.2921658T>A | GRCh37 |
| NC_000018.8:g.2911658T>A | NCBI36 |
| NG_007507.1:g.95288A>T , LRG_174:g.95288A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261596.9:c.2328-13A>T | ENSP00000261596.4:n.2328-13A>T | |
| ENST00000697039.1:c.2328-13A>T | ENSP00000513061.1:n.2328-13A>T | |
| ENST00000697040.1:c.2328-13A>T | ENSP00000513062.1:n.2328-13A>T | |
| ENST00000697041.1:c.1023-13A>T | ENSP00000513063.1:n.1023-13A>T | |
| ENST00000677752.1:c.2328-13A>T MANE Select | ENSP00000504857.1:n.2328-13A>T | |
| ENST00000261596.8:c.2328-13A>T | ENSP00000261596.4:n.2328-13A>T | |
| NM_014646.2:c.2328-13A>T , LRG_174t1:c.2328-13A>T | NP_055461.1:n.2328-13A>T | |
| XM_005258177.3:c.2439-13A>T | XP_005258234.1:n.2439-13A>T | |
| XM_005258178.2:c.2328-13A>T | XP_005258235.1:n.2328-13A>T | |
| XM_005258179.3:c.2328-13A>T | XP_005258236.1:n.2328-13A>T | |
| XM_005258177.4:c.2439-13A>T | XP_005258234.1:n.2439-13A>T | |
| XM_005258178.3:c.2328-13A>T | XP_005258235.1:n.2328-13A>T | |
| XM_005258179.5:c.2328-13A>T | XP_005258236.1:n.2328-13A>T | |
| XM_017026098.1:c.2328-13A>T | XP_016881587.1:n.2328-13A>T | |
| XM_017026099.1:c.2328-13A>T | XP_016881588.1:n.2328-13A>T | |
| NM_001375808.1:c.2328-13A>T | NP_001362737.1:n.2328-13A>T | |
| NM_001375809.1:c.2328-13A>T | NP_001362738.1:n.2328-13A>T | |
| NM_001375808.2:c.2328-13A>T MANE Select | NP_001362737.1:n.2328-13A>T |