Linked Data
ClinVar Variation Id:
290921
dbSNP Id:
rs535674229
ExAC:
18:2697888 C / T
gnomAD v2:
18-2697888-C-T
gnomAD v3:
18-2697890-C-T
gnomAD v4:
18-2697890-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.2697890C>T , CM000680.2:g.2697890C>T | GRCh38 |
| NC_000018.9:g.2697888C>T , CM000680.1:g.2697888C>T | GRCh37 |
| NC_000018.8:g.2687888C>T | NCBI36 |
| NG_031972.1:g.47003C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684915.1:n.1348C>T | ||
| ENST00000688342.1:c.1191C>T | ENSP00000508422.1:p.Asp397= | |
| ENST00000693213.1:n.469C>T | ||
| ENST00000320876.11:c.1191C>T MANE Select | ENSP00000326603.7:p.Asp397= | |
| ENST00000320876.10:c.1191C>T | ENSP00000326603.6:p.Asp397= | |
| NM_015295.2:c.1191C>T | NP_056110.2:p.Asp397= | |
| XM_011525642.1:c.1191C>T | XP_011523944.1:p.Asp397= | |
| XM_011525643.1:c.1191C>T | XP_011523945.1:p.Asp397= | |
| XM_011525644.1:c.807C>T | XP_011523946.1:p.Asp269= | |
| XM_011525645.1:c.627C>T | XP_011523947.1:p.Asp209= | |
| XM_011525646.1:c.1191C>T | XP_011523948.1:p.Asp397= | |
| XM_011525647.1:c.1191C>T | XP_011523949.1:p.Asp397= | |
| XR_430039.1:n.1380C>T | ||
| XR_935054.1:n.1380C>T | ||
| XR_935055.1:n.1380C>T | ||
| XM_011525643.2:c.1191C>T | XP_011523945.1:p.Asp397= | |
| XM_017025684.1:c.627C>T | XP_016881173.1:p.Asp209= | |
| XR_001753172.1:n.1380C>T | ||
| XR_001753173.1:n.1380C>T | ||
| XR_001753174.1:n.1380C>T | ||
| XR_001753175.1:n.1380C>T | ||
| XR_001753176.1:n.1380C>T | ||
| XR_001753177.1:n.1380C>T | ||
| XR_001753178.1:n.1380C>T | ||
| XR_001753179.1:n.1380C>T | ||
| XR_935055.2:n.1380C>T | ||
| NM_015295.3:c.1191C>T MANE Select | NP_056110.2:p.Asp397= |