Linked Data
ClinVar Variation Id:
457075
dbSNP Id:
rs747104878
ExAC:
20:32000136 G / A
gnomAD v2:
20-32000136-G-A
gnomAD v3:
20-33412330-G-A
gnomAD v4:
20-33412330-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.33412330G>A , CM000682.2:g.33412330G>A | GRCh38 |
| NC_000020.10:g.32000136G>A , CM000682.1:g.32000136G>A | GRCh37 |
| NC_000020.9:g.31463797G>A | NCBI36 |
| NG_011622.1:g.36563C>T , LRG_332:g.36563C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000217381.3:c.1006C>T MANE Select | ENSP00000217381.2:p.Arg336Trp | |
| ENST00000217381.2:c.1006C>T | ENSP00000217381.2:p.Arg336Trp | |
| NM_003098.2:c.1006C>T , LRG_332t1:c.1006C>T | NP_003089.1:p.Arg336Trp | |
| XM_005260517.1:c.1006C>T | XP_005260574.1:p.Arg336Trp | |
| XM_011529007.1:c.1006C>T | XP_011527309.1:p.Arg336Trp | |
| XM_011529008.1:c.1006C>T | XP_011527310.1:p.Arg336Trp | |
| XR_936612.1:n.1239C>T | ||
| XM_024451971.1:c.679C>T | XP_024307739.1:p.Arg227Trp | |
| NM_003098.3:c.1006C>T MANE Select | NP_003089.1:p.Arg336Trp |