Linked Data
ClinVar Variation Id:
2315566
ClinVar RCV Id:
RCV002919318
dbSNP Id:
rs776260316
ExAC:
16:56918047 T / G
gnomAD v2:
16-56918047-T-G
gnomAD v4:
16-56884135-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.56884135T>G , CM000678.2:g.56884135T>G | GRCh38 |
| NC_000016.9:g.56918047T>G , CM000678.1:g.56918047T>G | GRCh37 |
| NC_000016.8:g.55475548T>G | NCBI36 |
| NG_009386.1:g.23929T>G | |
| NG_009386.2:g.23929T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000563236.6:c.1756T>G MANE Select | ENSP00000456149.2:p.Trp586Gly | |
| ENST00000262502.5:c.1753T>G | ENSP00000262502.5:p.Trp585Gly | |
| ENST00000438926.6:c.1756T>G | ENSP00000402152.2:p.Trp586Gly | |
| ENST00000563236.5:c.1756T>G | ENSP00000456149.1:p.Trp586Gly | |
| ENST00000566786.5:c.1753T>G | ENSP00000457552.1:p.Trp585Gly | |
| NM_000339.2:c.1756T>G | NP_000330.2:p.Trp586Gly | |
| NM_001126107.1:c.1753T>G | NP_001119579.1:p.Trp585Gly | |
| NM_001126108.1:c.1756T>G | NP_001119580.1:p.Trp586Gly | |
| XM_005256119.1:c.1753T>G | XP_005256176.1:p.Trp585Gly | |
| XM_005256119.2:c.1753T>G | XP_005256176.1:p.Trp585Gly | |
| NM_000339.3:c.1756T>G | NP_000330.3:p.Trp586Gly | |
| NM_001126107.2:c.1753T>G | NP_001119579.2:p.Trp585Gly | |
| NM_001126108.2:c.1756T>G MANE Select | NP_001119580.2:p.Trp586Gly |