Linked Data
ClinVar Variation Id:
67461
dbSNP Id:
rs199473019
ExAC:
7:150644554 C / T
gnomAD v2:
7-150644554-C-T
gnomAD v3:
7-150947466-C-T
gnomAD v4:
7-150947466-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.150947466C>T , CM000669.2:g.150947466C>T | GRCh38 |
| NC_000007.13:g.150644554C>T , CM000669.1:g.150644554C>T | GRCh37 |
| NC_000007.12:g.150275487C>T | NCBI36 |
| NG_008916.1:g.35461G>A , LRG_288:g.35461G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000684241.1:n.3847G>A | ||
| ENST00000262186.10:c.3014G>A MANE Select | ENSP00000262186.5:p.Arg1005Gln | |
| ENST00000330883.9:c.1994G>A | ENSP00000328531.4:p.Arg665Gln | |
| ENST00000262186.9:c.3014G>A | ENSP00000262186.5:p.Arg1005Gln | |
| ENST00000330883.8:c.1994G>A | ENSP00000328531.4:p.Arg665Gln | |
| NM_000238.3:c.3014G>A , LRG_288t1:c.3014G>A | NP_000229.1:p.Arg1005Gln | |
| NM_172057.2:c.1994G>A , LRG_288t3:c.1994G>A | NP_742054.1:p.Arg665Gln | |
| XM_011516185.1:c.2714G>A | XP_011514487.1:p.Arg905Gln | |
| XM_011516186.1:c.*94G>A | XP_011514488.1:n.*94G>A | |
| XM_011516185.2:c.2714G>A | XP_011514487.1:p.Arg905Gln | |
| XM_011516186.3:c.*94G>A | XP_011514488.1:n.*94G>A | |
| XM_017012195.1:c.2864G>A | XP_016867684.1:p.Arg955Gln | |
| XM_017012196.1:c.2837G>A | XP_016867685.1:p.Arg946Gln | |
| NM_000238.4:c.3014G>A MANE Select | NP_000229.1:p.Arg1005Gln | |
| NM_172057.3:c.1994G>A | NP_742054.1:p.Arg665Gln |