Linked Data
ClinVar Variation Id:
316997
dbSNP Id:
rs146980624
ExAC:
15:68506712 G / C
gnomAD v2:
15-68506712-G-C
gnomAD v3:
15-68214374-G-C
gnomAD v4:
15-68214374-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.68214374G>C , CM000677.2:g.68214374G>C | GRCh38 |
| NC_000015.9:g.68506712G>C , CM000677.1:g.68506712G>C | GRCh37 |
| NC_000015.8:g.66293766G>C | NCBI36 |
| NG_008764.2:g.47838C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000249806.11:c.213C>G MANE Select | ENSP00000249806.5:p.Leu71= | |
| ENST00000562767.2:c.83+15128C>G | ENSP00000456336.1:n.83+15128C>G | |
| ENST00000563917.2:n.55C>G | ||
| ENST00000565471.6:c.84-4615C>G | ENSP00000457384.1:n.84-4615C>G | |
| ENST00000635747.1:c.*116C>G | ENSP00000490627.1:n.*116C>G | |
| ENST00000635754.1:n.1235C>G | ||
| ENST00000636020.1:n.345C>G | ||
| ENST00000636212.1:c.213C>G | ENSP00000489851.1:p.Leu71= | |
| ENST00000636314.1:c.98C>G | ENSP00000490295.1:p.Ser33Trp | |
| ENST00000637054.1:c.198+4162C>G | ENSP00000490807.1:n.198+4162C>G | |
| ENST00000637223.1:c.*116C>G | ENSP00000490010.1:n.*116C>G | |
| ENST00000637329.1:c.124C>G | ||
| ENST00000637450.1:c.98C>G | ENSP00000490204.1:p.Ser33Trp | |
| ENST00000637494.1:c.199-3056C>G | ENSP00000490057.1:n.199-3056C>G | |
| ENST00000637667.1:c.199-2511C>G | ENSP00000489843.1:n.199-2511C>G | |
| ENST00000637823.1:c.139C>G | ||
| ENST00000637888.1:c.198+4162C>G | ENSP00000490546.1:n.198+4162C>G | |
| ENST00000638076.1:c.213C>G | ENSP00000490373.1:p.Leu71= | |
| ENST00000638144.1:n.45C>G | ||
| ENST00000646164.1:c.38+4162C>G | ||
| ENST00000249806.9:c.213C>G | ENSP00000249806.5:p.Leu71= | |
| ENST00000538696.5:c.309C>G | ENSP00000445770.1:p.Leu103= | |
| ENST00000562767.1:c.83+15128C>G | ENSP00000456336.1:n.83+15128C>G | |
| ENST00000564752.1:c.213C>G | ENSP00000457822.1:p.Leu71= | |
| ENST00000564846.1:n.645C>G | ||
| ENST00000565471.5:c.84-4615C>G | ENSP00000457384.1:n.84-4615C>G | |
| ENST00000566347.5:c.213C>G | ENSP00000457783.1:p.Leu71= | |
| ENST00000567060.5:c.213C>G | ENSP00000454818.1:p.Leu71= | |
| NM_017882.2:c.213C>G | NP_060352.1:p.Leu71= | |
| XR_931861.1:n.316C>G | ||
| NM_017882.3:c.213C>G MANE Select | NP_060352.1:p.Leu71= |