Linked Data
ClinVar Variation Id:
389293
dbSNP Id:
rs375091035
ExAC:
9:304653 G / A
gnomAD v2:
9-304653-G-A
gnomAD v3:
9-304653-G-A
gnomAD v4:
9-304653-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.304653G>A , CM000671.2:g.304653G>A | GRCh38 |
| NC_000009.11:g.304653G>A , CM000671.1:g.304653G>A | GRCh37 |
| NC_000009.10:g.294653G>A | NCBI36 |
| NG_017007.1:g.94789G>A , LRG_196:g.94789G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382329.2:c.273G>A | ENSP00000371766.2:p.Pro91= | |
| ENST00000483757.6:c.273G>A | ENSP00000417691.2:p.Pro91= | |
| ENST00000682249.1:c.273G>A | ENSP00000507731.1:p.Pro91= | |
| ENST00000684384.1:n.586G>A | ||
| ENST00000432829.7:c.477G>A MANE Select | ENSP00000394888.3:p.Pro159= | |
| ENST00000382341.5:n.372G>A | ||
| ENST00000432829.6:c.477G>A | ENSP00000394888.3:p.Pro159= | |
| ENST00000453981.5:c.273G>A | ENSP00000408464.2:p.Pro91= | |
| ENST00000454469.6:n.586G>A | ||
| ENST00000469391.5:c.273G>A | ENSP00000419438.1:p.Pro91= | |
| ENST00000478380.5:n.356G>A | ||
| ENST00000483757.5:c.273G>A | ENSP00000417691.1:p.Pro91= | |
| ENST00000487230.5:c.273G>A | ENSP00000418318.1:p.Pro91= | |
| ENST00000495184.5:n.338G>A | ||
| ENST00000524396.5:c.*440G>A | ENSP00000436628.1:n.*440G>A | |
| NM_001190458.1:c.273G>A | NP_001177387.1:p.Pro91= | |
| NM_001193536.1:c.273G>A | NP_001180465.1:p.Pro91= | |
| NM_203447.3:c.477G>A , LRG_196t1:c.477G>A | NP_982272.2:p.Pro159= | |
| XM_011518045.1:c.273G>A | XP_011516347.1:p.Pro91= | |
| XM_011518046.1:c.339G>A | XP_011516348.1:p.Pro113= | |
| XM_011518047.1:c.273G>A | XP_011516349.1:p.Pro91= | |
| XM_011518048.1:c.273G>A | XP_011516350.1:p.Pro91= | |
| XM_011518045.3:c.273G>A | XP_011516347.1:p.Pro91= | |
| XM_011518046.2:c.339G>A | XP_011516348.1:p.Pro113= | |
| XM_011518047.3:c.273G>A | XP_011516349.1:p.Pro91= | |
| XM_011518048.2:c.273G>A | XP_011516350.1:p.Pro91= | |
| XM_017015173.1:c.273G>A | XP_016870662.1:p.Pro91= | |
| XM_017015174.1:c.339G>A | XP_016870663.1:p.Pro113= | |
| NM_001190458.2:c.273G>A | NP_001177387.1:p.Pro91= | |
| NM_001193536.2:c.273G>A | NP_001180465.1:p.Pro91= | |
| NM_203447.4:c.477G>A MANE Select | NP_982272.2:p.Pro159= |