Linked Data
ClinVar Variation Id:
213380
dbSNP Id:
rs151329128
ExAC:
5:127800456 G / A
gnomAD v2:
5-127800456-G-A
gnomAD v3:
5-128464763-G-A
gnomAD v4:
5-128464763-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128464763G>A , CM000667.2:g.128464763G>A | GRCh38 |
| NC_000005.9:g.127800456G>A , CM000667.1:g.127800456G>A | GRCh37 |
| NC_000005.8:g.127828355G>A | NCBI36 |
| NG_008750.1:g.78280C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000508053.6:c.787C>T | ENSP00000424571.2:p.Arg263Trp | |
| ENST00000703787.1:n.494C>T | ||
| ENST00000262464.9:c.787C>T MANE Select | ENSP00000262464.4:p.Arg263Trp | |
| ENST00000262464.8:c.787C>T | ENSP00000262464.4:p.Arg263Trp | |
| ENST00000502468.5:c.787C>T | ENSP00000424753.1:p.Arg263Trp | |
| ENST00000508053.5:c.787C>T | ENSP00000424571.1:p.Arg263Trp | |
| ENST00000508989.5:c.688C>T | ENSP00000425596.1:p.Arg230Trp | |
| ENST00000514742.1:n.1407C>T | ||
| ENST00000619499.4:c.784C>T | ENSP00000482132.1:p.Arg262Trp | |
| ENST00000620257.1:c.787C>T | ENSP00000479157.1:p.Arg263Trp | |
| NM_001999.3:c.787C>T | NP_001990.2:p.Arg263Trp | |
| XM_017009228.2:c.787C>T | XP_016864717.1:p.Arg263Trp | |
| NM_001999.4:c.787C>T MANE Select | NP_001990.2:p.Arg263Trp |