Linked Data
ClinVar Variation Id:
380424
ClinVar RCV Id:
RCV000429959
dbSNP Id:
rs753497587
ExAC:
15:68510983 C / G
gnomAD v2:
15-68510983-C-G
gnomAD v4:
15-68218645-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.68218645C>G , CM000677.2:g.68218645C>G | GRCh38 |
| NC_000015.9:g.68510983C>G , CM000677.1:g.68510983C>G | GRCh37 |
| NC_000015.8:g.66298037C>G | NCBI36 |
| NG_008764.2:g.43567G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000249806.11:c.89G>C MANE Select | ENSP00000249806.5:p.Gly30Ala | |
| ENST00000562767.2:c.83+10857G>C | ENSP00000456336.1:n.83+10857G>C | |
| ENST00000563917.2:n.41-4257G>C | ||
| ENST00000565471.6:c.84-8886G>C | ENSP00000457384.1:n.84-8886G>C | |
| ENST00000635747.1:c.178G>C | ENSP00000490627.1:p.Ala60Pro | |
| ENST00000636020.1:n.221G>C | ||
| ENST00000636212.1:c.89G>C | ENSP00000489851.1:p.Gly30Ala | |
| ENST00000636314.1:c.84-4257G>C | ENSP00000490295.1:n.84-4257G>C | |
| ENST00000636876.1:c.*109G>C | ENSP00000489950.1:n.*109G>C | |
| ENST00000637054.1:c.89G>C | ENSP00000490807.1:p.Gly30Ala | |
| ENST00000637223.1:c.178G>C | ENSP00000490010.1:p.Ala60Pro | |
| ENST00000637450.1:c.84-4257G>C | ENSP00000490204.1:n.84-4257G>C | |
| ENST00000637494.1:c.89G>C | ENSP00000490057.1:p.Gly30Ala | |
| ENST00000637667.1:c.89G>C | ENSP00000489843.1:p.Gly30Ala | |
| ENST00000637823.1:c.15G>C | ||
| ENST00000637888.1:c.89G>C | ENSP00000490546.1:p.Gly30Ala | |
| ENST00000638076.1:c.89G>C | ENSP00000490373.1:p.Gly30Ala | |
| ENST00000638144.1:n.31-4257G>C | ||
| ENST00000249806.9:c.89G>C | ENSP00000249806.5:p.Gly30Ala | |
| ENST00000538696.5:c.185G>C | ENSP00000445770.1:p.Gly62Ala | |
| ENST00000562767.1:c.83+10857G>C | ENSP00000456336.1:n.83+10857G>C | |
| ENST00000564752.1:c.89G>C | ENSP00000457822.1:p.Gly30Ala | |
| ENST00000564846.1:n.521G>C | ||
| ENST00000565471.5:c.84-8886G>C | ENSP00000457384.1:n.84-8886G>C | |
| ENST00000566347.5:c.89G>C | ENSP00000457783.1:p.Gly30Ala | |
| ENST00000567060.5:c.89G>C | ENSP00000454818.1:p.Gly30Ala | |
| ENST00000569336.1:n.175G>C | ||
| NM_017882.2:c.89G>C | NP_060352.1:p.Gly30Ala | |
| XR_931861.1:n.192G>C | ||
| NM_017882.3:c.89G>C MANE Select | NP_060352.1:p.Gly30Ala |