Linked Data
ClinVar Variation Id:
1784074
dbSNP Id:
rs202011408
gnomAD v2:
10-112572152-G-A
gnomAD v3:
10-110812394-G-A
gnomAD v4:
10-110812394-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110812394G>A , CM000672.2:g.110812394G>A | GRCh38 |
| NC_000010.10:g.112572152G>A , CM000672.1:g.112572152G>A | GRCh37 |
| NC_000010.9:g.112562142G>A | NCBI36 |
| NG_021177.1:g.172998G>A , LRG_382:g.172998G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369519.4:c.1997G>A MANE Select | ENSP00000358532.3:p.Arg666Gln | |
| ENST00000369519.3:c.1997G>A | ENSP00000358532.3:p.Arg666Gln | |
| NM_001134363.2:c.1997G>A | NP_001127835.2:p.Arg666Gln | |
| XM_011539697.1:c.1613G>A | XP_011537999.1:p.Arg538Gln | |
| XM_017016103.2:c.1832G>A | XP_016871592.1:p.Arg611Gln | |
| XM_017016104.2:c.1613G>A | XP_016871593.1:p.Arg538Gln | |
| NM_001134363.3:c.1997G>A MANE Select | NP_001127835.2:p.Arg666Gln |