Linked Data
ClinVar Variation Id:
338764
ClinVar RCV Id:
RCV002520020
dbSNP Id:
rs17802735
ExAC:
20:50405502 C / T
gnomAD v2:
20-50405502-C-T
gnomAD v3:
20-51788963-C-T
gnomAD v4:
20-51788963-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.51788963C>T , CM000682.2:g.51788963C>T | GRCh38 |
| NC_000020.10:g.50405502C>T , CM000682.1:g.50405502C>T | GRCh37 |
| NC_000020.9:g.49838909C>T | NCBI36 |
| NG_008000.1:g.18547G>A , LRG_675:g.18547G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000217086.9:c.2640G>A MANE Select | ENSP00000217086.4:p.Ser880= | |
| ENST00000217086.8:c.2640G>A | ENSP00000217086.4:p.Ser880= | |
| ENST00000371539.7:c.309G>A | ENSP00000360594.3:p.Ser103= | |
| ENST00000395997.3:c.1329G>A | ENSP00000379319.3:p.Ser443= | |
| NM_020436.3:c.2640G>A , LRG_675t1:c.2640G>A | NP_065169.1:p.Ser880= | |
| XM_005260467.2:c.2334G>A | XP_005260524.1:p.Ser778= | |
| XM_006723834.2:c.2334G>A | XP_006723897.1:p.Ser778= | |
| XM_011528919.1:c.2514G>A | XP_011527221.1:p.Ser838= | |
| XM_011528920.1:c.2334G>A | XP_011527222.1:p.Ser778= | |
| XM_011528921.1:c.2334G>A | XP_011527223.1:p.Ser778= | |
| XM_011528922.1:c.2334G>A | XP_011527224.1:p.Ser778= | |
| XM_011528923.1:c.1329G>A | XP_011527225.1:p.Ser443= | |
| NM_001318031.1:c.1329G>A | NP_001304960.1:p.Ser443= | |
| NM_020436.4:c.2640G>A | NP_065169.1:p.Ser880= | |
| XM_005260467.4:c.2334G>A | XP_005260524.1:p.Ser778= | |
| XM_011528921.2:c.2334G>A | XP_011527223.1:p.Ser778= | |
| XM_011528922.2:c.2334G>A | XP_011527224.1:p.Ser778= | |
| NM_020436.5:c.2640G>A MANE Select | NP_065169.1:p.Ser880= | |
| NM_001318031.2:c.1329G>A | NP_001304960.1:p.Ser443= |