Linked Data
ClinVar Variation Id:
142692
dbSNP Id:
rs587782647
ExAC:
16:68835678 G / A
gnomAD v2:
16-68835678-G-A
gnomAD v3:
16-68801775-G-A
gnomAD v4:
16-68801775-G-A
COSMIC:
COSM4384876
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.68801775G>A , CM000678.2:g.68801775G>A | GRCh38 |
| NC_000016.9:g.68835678G>A , CM000678.1:g.68835678G>A | GRCh37 |
| NC_000016.8:g.67393179G>A | NCBI36 |
| NG_008021.1:g.69484G>A , LRG_301:g.69484G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261769.10:c.269G>A MANE Select | ENSP00000261769.4:p.Arg90Gln | |
| ENST00000261769.9:c.269G>A | ENSP00000261769.4:p.Arg90Gln | |
| ENST00000422392.6:c.269G>A | ENSP00000414946.2:p.Arg90Gln | |
| ENST00000561751.1:c.36G>A | ||
| ENST00000562836.5:n.340G>A | ||
| ENST00000564676.5:n.551G>A | ||
| ENST00000564745.1:n.264G>A | ||
| ENST00000566510.5:c.269G>A | ENSP00000458139.1:p.Arg90Gln | |
| ENST00000566612.5:c.269G>A | ENSP00000454782.1:p.Arg90Gln | |
| ENST00000611625.4:c.269G>A | ENSP00000481063.1:p.Arg90Gln | |
| ENST00000612417.4:c.269G>A | ENSP00000478360.1:p.Arg90Gln | |
| ENST00000621016.4:c.269G>A | ENSP00000480664.1:p.Arg90Gln | |
| NM_004360.3:c.269G>A , LRG_301t1:c.269G>A | NP_004351.1:p.Arg90Gln | |
| XM_011523488.1:c.-467G>A | XP_011521790.1:n.-467G>A | |
| XM_011523489.1:c.-467G>A | XP_011521791.1:n.-467G>A | |
| NM_001317184.1:c.269G>A | NP_001304113.1:p.Arg90Gln | |
| NM_001317185.1:c.-1347G>A | NP_001304114.1:n.-1347G>A | |
| NM_001317186.1:c.-1551G>A | NP_001304115.1:n.-1551G>A | |
| NM_004360.4:c.269G>A | NP_004351.1:p.Arg90Gln | |
| NM_004360.5:c.269G>A MANE Select | NP_004351.1:p.Arg90Gln | |
| NM_001317184.2:c.269G>A | NP_001304113.1:p.Arg90Gln | |
| NM_001317185.2:c.-1347G>A | NP_001304114.1:n.-1347G>A | |
| NM_001317186.2:c.-1551G>A | NP_001304115.1:n.-1551G>A |