Linked Data
ClinVar Variation Id:
252416
dbSNP Id:
rs80359129
gnomAD v2:
13-32950876-G-T
gnomAD v4:
13-32376739-G-T
PubMed:
PMID:26295337
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.32376739G>T , CM000675.2:g.32376739G>T | GRCh38 |
| NC_000013.10:g.32950876G>T , CM000675.1:g.32950876G>T | GRCh37 |
| NC_000013.9:g.31848876G>T | NCBI36 |
| NG_012772.3:g.66260G>T , LRG_293:g.66260G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000470094.2:c.8702G>T | ENSP00000434898.2:p.Gly2901Val | |
| ENST00000528762.2:c.*69G>T | ENSP00000433168.2:n.*69G>T | |
| ENST00000530893.7:c.8333G>T | ENSP00000499438.2:p.Gly2778Val | |
| ENST00000665585.2:c.*264G>T | ENSP00000499570.2:n.*264G>T | |
| ENST00000666593.2:c.8702G>T | ENSP00000499256.2:p.Gly2901Val | |
| ENST00000700202.2:c.8702G>T | ENSP00000514856.2:p.Gly2901Val | |
| ENST00000700202.1:c.1169G>T | ENSP00000514856.1:p.Gly390Val | |
| ENST00000700203.1:n.829G>T | ||
| ENST00000380152.8:c.8702G>T MANE Select | ENSP00000369497.3:p.Gly2901Val | |
| ENST00000544455.6:c.8702G>T | ENSP00000439902.1:p.Gly2901Val | |
| ENST00000614259.2:c.8710G>T | ENSP00000506251.1:n.8710G>T | |
| ENST00000665585.1:c.1580G>T | ||
| ENST00000680887.1:c.8702G>T | ENSP00000505508.1:p.Gly2901Val | |
| ENST00000380152.7:c.8702G>T | ENSP00000369497.3:p.Gly2901Val | |
| ENST00000528762.1:c.264G>T | ENSP00000433168.1:n.264G>T | |
| ENST00000544455.5:c.8702G>T | ENSP00000439902.1:p.Gly2901Val | |
| NM_000059.3:c.8702G>T , LRG_293t1:c.8702G>T | NP_000050.2:p.Gly2901Val | |
| XM_011535203.1:c.8702G>T | XP_011533505.1:p.Gly2901Val | |
| XM_011535204.1:c.8606G>T | XP_011533506.1:p.Gly2869Val | |
| XM_011535205.1:c.8702G>T | XP_011533507.1:p.Gly2901Val | |
| NM_000059.4:c.8702G>T MANE Select | NP_000050.3:p.Gly2901Val |