Linked Data
ClinVar Variation Id:
30689
ClinVar RCV Id:
RCV000023667
dbSNP Id:
rs387906976
PubMed:
PMID:21224894
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.4417180C>A , CM000665.2:g.4417180C>A | GRCh38 |
| NC_000003.11:g.4458864C>A , CM000665.1:g.4458864C>A | GRCh37 |
| NC_000003.10:g.4433864C>A | NCBI36 |
| NG_016225.1:g.55103G>T | |
| NG_016225.2:g.55103G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272902.10:c.788G>T MANE Select | ENSP00000272902.5:p.Gly263Val | |
| ENST00000272902.9:c.788G>T | ENSP00000272902.5:p.Gly263Val | |
| ENST00000383843.9:c.713G>T | ENSP00000373355.5:p.Gly238Val | |
| ENST00000405420.2:c.788G>T | ENSP00000384977.2:p.Gly263Val | |
| ENST00000448413.5:c.788G>T | ENSP00000404384.1:p.Gly263Val | |
| ENST00000458465.6:c.445-6202G>T | ENSP00000410060.2:n.445-6202G>T | |
| NM_001164674.1:c.713G>T | NP_001158146.1:p.Gly238Val | |
| NM_001164675.1:c.788G>T | NP_001158147.1:p.Gly263Val | |
| NM_182760.3:c.788G>T | NP_877437.2:p.Gly263Val | |
| XM_011533623.1:c.788G>T | XP_011531925.1:p.Gly263Val | |
| XM_011533624.1:c.788G>T | XP_011531926.1:p.Gly263Val | |
| XM_011533625.1:c.788G>T | XP_011531927.1:p.Gly263Val | |
| XM_011533626.1:c.788G>T | XP_011531928.1:p.Gly263Val | |
| XM_011533624.3:c.788G>T | XP_011531926.1:p.Gly263Val | |
| XM_011533625.3:c.788G>T | XP_011531927.1:p.Gly263Val | |
| XM_011533626.3:c.788G>T | XP_011531928.1:p.Gly263Val | |
| XM_017006252.2:c.788G>T | XP_016861741.1:p.Gly263Val | |
| XM_017006253.1:c.713G>T | XP_016861742.1:p.Gly238Val | |
| XM_017006254.2:c.788G>T | XP_016861743.1:p.Gly263Val | |
| XM_017006255.2:c.788G>T | XP_016861744.1:p.Gly263Val | |
| NM_182760.4:c.788G>T MANE Select | NP_877437.2:p.Gly263Val | |
| NM_001164674.2:c.713G>T | NP_001158146.1:p.Gly238Val | |
| NM_001164675.2:c.788G>T | NP_001158147.1:p.Gly263Val |