Linked Data
ClinVar Variation Id:
834684
ClinVar RCV Id:
RCV001035421
dbSNP Id:
rs35606263
ExAC:
16:68835623 G / C
gnomAD v2:
16-68835623-G-C
gnomAD v4:
16-68801720-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.68801720G>C , CM000678.2:g.68801720G>C | GRCh38 |
| NC_000016.9:g.68835623G>C , CM000678.1:g.68835623G>C | GRCh37 |
| NC_000016.8:g.67393124G>C | NCBI36 |
| NG_008021.1:g.69429G>C , LRG_301:g.69429G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261769.10:c.214G>C MANE Select | ENSP00000261769.4:p.Asp72His | |
| ENST00000261769.9:c.214G>C | ENSP00000261769.4:p.Asp72His | |
| ENST00000422392.6:c.214G>C | ENSP00000414946.2:p.Asp72His | |
| ENST00000562836.5:n.285G>C | ||
| ENST00000564676.5:n.496G>C | ||
| ENST00000564745.1:n.209G>C | ||
| ENST00000566510.5:c.214G>C | ENSP00000458139.1:p.Asp72His | |
| ENST00000566612.5:c.214G>C | ENSP00000454782.1:p.Asp72His | |
| ENST00000611625.4:c.214G>C | ENSP00000481063.1:p.Asp72His | |
| ENST00000612417.4:c.214G>C | ENSP00000478360.1:p.Asp72His | |
| ENST00000621016.4:c.214G>C | ENSP00000480664.1:p.Asp72His | |
| NM_004360.3:c.214G>C , LRG_301t1:c.214G>C | NP_004351.1:p.Asp72His | |
| XM_011523488.1:c.-522G>C | XP_011521790.1:n.-522G>C | |
| XM_011523489.1:c.-522G>C | XP_011521791.1:n.-522G>C | |
| NM_001317184.1:c.214G>C | NP_001304113.1:p.Asp72His | |
| NM_001317185.1:c.-1402G>C | NP_001304114.1:n.-1402G>C | |
| NM_001317186.1:c.-1606G>C | NP_001304115.1:n.-1606G>C | |
| NM_004360.4:c.214G>C | NP_004351.1:p.Asp72His | |
| NM_004360.5:c.214G>C MANE Select | NP_004351.1:p.Asp72His | |
| NM_001317184.2:c.214G>C | NP_001304113.1:p.Asp72His | |
| NM_001317185.2:c.-1402G>C | NP_001304114.1:n.-1402G>C | |
| NM_001317186.2:c.-1606G>C | NP_001304115.1:n.-1606G>C |