Linked Data
ClinVar Variation Id:
190934
dbSNP Id:
rs786205848
gnomAD v2:
20-32031267-C-G
gnomAD v3:
20-33443461-C-G
gnomAD v4:
20-33443461-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.33443461C>G , CM000682.2:g.33443461C>G | GRCh38 |
| NC_000020.10:g.32031267C>G , CM000682.1:g.32031267C>G | GRCh37 |
| NC_000020.9:g.31494928C>G | NCBI36 |
| NG_011622.1:g.5432G>C , LRG_332:g.5432G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000217381.3:c.160G>C MANE Select | ENSP00000217381.2:p.Gly54Arg | |
| ENST00000217381.2:c.160G>C | ENSP00000217381.2:p.Gly54Arg | |
| NM_003098.2:c.160G>C , LRG_332t1:c.160G>C | NP_003089.1:p.Gly54Arg | |
| XM_005260517.1:c.160G>C | XP_005260574.1:p.Gly54Arg | |
| XM_011529007.1:c.160G>C | XP_011527309.1:p.Gly54Arg | |
| XM_011529008.1:c.160G>C | XP_011527310.1:p.Gly54Arg | |
| XR_936612.1:n.393G>C | ||
| NM_003098.3:c.160G>C MANE Select | NP_003089.1:p.Gly54Arg |