Linked Data
ClinVar Variation Id:
260642
dbSNP Id:
rs369550628
ExAC:
18:2666894 C / T
gnomAD v2:
18-2666894-C-T
gnomAD v3:
18-2666895-C-T
gnomAD v4:
18-2666895-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.2666895C>T , CM000680.2:g.2666895C>T | GRCh38 |
| NC_000018.9:g.2666894C>T , CM000680.1:g.2666894C>T | GRCh37 |
| NC_000018.8:g.2656894C>T | NCBI36 |
| NG_031972.1:g.16009C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684915.1:n.445C>T | ||
| ENST00000688342.1:c.288C>T | ENSP00000508422.1:p.Thr96= | |
| ENST00000320876.11:c.288C>T MANE Select | ENSP00000326603.7:p.Thr96= | |
| ENST00000320876.10:c.288C>T | ENSP00000326603.6:p.Thr96= | |
| NM_015295.2:c.288C>T | NP_056110.2:p.Thr96= | |
| XM_011525642.1:c.288C>T | XP_011523944.1:p.Thr96= | |
| XM_011525643.1:c.288C>T | XP_011523945.1:p.Thr96= | |
| XM_011525644.1:c.-97C>T | XP_011523946.1:n.-97C>T | |
| XM_011525646.1:c.288C>T | XP_011523948.1:p.Thr96= | |
| XM_011525647.1:c.288C>T | XP_011523949.1:p.Thr96= | |
| XR_430039.1:n.477C>T | ||
| XR_935054.1:n.477C>T | ||
| XR_935055.1:n.477C>T | ||
| XM_011525643.2:c.288C>T | XP_011523945.1:p.Thr96= | |
| XM_017025684.1:c.-455C>T | XP_016881173.1:n.-455C>T | |
| XR_001753172.1:n.477C>T | ||
| XR_001753173.1:n.477C>T | ||
| XR_001753174.1:n.477C>T | ||
| XR_001753175.1:n.477C>T | ||
| XR_001753176.1:n.477C>T | ||
| XR_001753177.1:n.477C>T | ||
| XR_001753178.1:n.477C>T | ||
| XR_001753179.1:n.477C>T | ||
| XR_935055.2:n.477C>T | ||
| NM_015295.3:c.288C>T MANE Select | NP_056110.2:p.Thr96= |