Linked Data
ClinVar Variation Id:
225722
dbSNP Id:
rs373697701
gnomAD v2:
13-32954289-C-T
gnomAD v4:
13-32380152-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.32380152C>T , CM000675.2:g.32380152C>T | GRCh38 |
| NC_000013.10:g.32954289C>T , CM000675.1:g.32954289C>T | GRCh37 |
| NC_000013.9:g.31852289C>T | NCBI36 |
| NG_012772.3:g.69673C>T , LRG_293:g.69673C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000470094.2:c.9256+7C>T | ENSP00000434898.2:n.9256+7C>T | |
| ENST00000528762.2:c.*623+7C>T | ENSP00000433168.2:n.*623+7C>T | |
| ENST00000530893.7:c.8887+7C>T | ENSP00000499438.2:n.8887+7C>T | |
| ENST00000665585.2:c.*818+7C>T | ENSP00000499570.2:n.*818+7C>T | |
| ENST00000666593.2:c.9256+7C>T | ENSP00000499256.2:n.9256+7C>T | |
| ENST00000700202.2:c.9205+7C>T | ENSP00000514856.2:n.9205+7C>T | |
| ENST00000700202.1:c.1672+7C>T | ENSP00000514856.1:n.1672+7C>T | |
| ENST00000700203.1:n.1383+7C>T | ||
| ENST00000380152.8:c.9256+7C>T MANE Select | ENSP00000369497.3:n.9256+7C>T | |
| ENST00000544455.6:c.9256+7C>T | ENSP00000439902.1:n.9256+7C>T | |
| ENST00000614259.2:c.9264+7C>T | ENSP00000506251.1:n.9264+7C>T | |
| ENST00000665585.1:c.2134+7C>T | ||
| ENST00000666593.1:c.139+7C>T | ENSP00000499256.1:n.139+7C>T | |
| ENST00000680887.1:c.9256+7C>T | ENSP00000505508.1:n.9256+7C>T | |
| ENST00000380152.7:c.9256+7C>T | ENSP00000369497.3:n.9256+7C>T | |
| ENST00000470094.1:c.213+7C>T | ||
| ENST00000544455.5:c.9256+7C>T | ENSP00000439902.1:n.9256+7C>T | |
| NM_000059.3:c.9256+7C>T , LRG_293t1:c.9256+7C>T | NP_000050.2:n.9256+7C>T | |
| XM_011535203.1:c.9256+7C>T | XP_011533505.1:n.9256+7C>T | |
| XM_011535204.1:c.9160+7C>T | XP_011533506.1:n.9160+7C>T | |
| NM_000059.4:c.9256+7C>T MANE Select | NP_000050.3:n.9256+7C>T |