Linked Data
ClinVar Variation Id:
463794
ClinVar RCV Id:
RCV000546498
dbSNP Id:
rs876660861
gnomAD v4:
16-68810330-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.68810330G>T , CM000678.2:g.68810330G>T | GRCh38 |
| NC_000016.9:g.68844233G>T , CM000678.1:g.68844233G>T | GRCh37 |
| NC_000016.8:g.67401734G>T | NCBI36 |
| NG_008021.1:g.78039G>T , LRG_301:g.78039G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261769.10:c.821G>T MANE Select | ENSP00000261769.4:p.Gly274Val | |
| ENST00000261769.9:c.821G>T | ENSP00000261769.4:p.Gly274Val | |
| ENST00000422392.6:c.821G>T | ENSP00000414946.2:p.Gly274Val | |
| ENST00000561751.1:c.455-1354G>T | ||
| ENST00000562836.5:n.892G>T | ||
| ENST00000566510.5:c.665G>T | ENSP00000458139.1:p.Gly222Val | |
| ENST00000566612.5:c.821G>T | ENSP00000454782.1:p.Gly274Val | |
| ENST00000611625.4:c.821G>T | ENSP00000481063.1:p.Gly274Val | |
| ENST00000612417.4:c.821G>T | ENSP00000478360.1:p.Gly274Val | |
| ENST00000621016.4:c.821G>T | ENSP00000480664.1:p.Gly274Val | |
| NM_004360.3:c.821G>T , LRG_301t1:c.821G>T | NP_004351.1:p.Gly274Val | |
| XM_011523488.1:c.86G>T | XP_011521790.1:p.Gly29Val | |
| XM_011523489.1:c.86G>T | XP_011521791.1:p.Gly29Val | |
| NM_001317184.1:c.821G>T | NP_001304113.1:p.Gly274Val | |
| NM_001317185.1:c.-795G>T | NP_001304114.1:n.-795G>T | |
| NM_001317186.1:c.-999G>T | NP_001304115.1:n.-999G>T | |
| NM_004360.4:c.821G>T | NP_004351.1:p.Gly274Val | |
| NM_004360.5:c.821G>T MANE Select | NP_004351.1:p.Gly274Val | |
| NM_001317184.2:c.821G>T | NP_001304113.1:p.Gly274Val | |
| NM_001317185.2:c.-795G>T | NP_001304114.1:n.-795G>T | |
| NM_001317186.2:c.-999G>T | NP_001304115.1:n.-999G>T |