Linked Data
ClinVar Variation Id:
68338
dbSNP Id:
rs199474732
gnomAD v3:
17-31233115-C-T
gnomAD v4:
17-31233115-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.31233115C>T , CM000679.2:g.31233115C>T | GRCh38 |
| NC_000017.10:g.29560133C>T , CM000679.1:g.29560133C>T | GRCh37 |
| NC_000017.9:g.26584259C>T | NCBI36 |
| NG_009018.1:g.143139C>T , LRG_214:g.143139C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696138.1:c.3655C>T | ENSP00000512431.1:p.Arg1219Trp | |
| ENST00000696139.1:c.955C>T | ENSP00000512432.1:p.Arg319Trp | |
| ENST00000691014.1:c.3640C>T | ENSP00000510595.1:p.Arg1214Trp | |
| ENST00000693210.1:n.336C>T | ||
| ENST00000358273.9:c.3610C>T MANE Select | ENSP00000351015.4:p.Arg1204Trp | |
| ENST00000356175.7:c.3610C>T | ENSP00000348498.3:p.Arg1204Trp | |
| ENST00000358273.8:c.3610C>T | ENSP00000351015.4:p.Arg1204Trp | |
| ENST00000456735.6:c.2608C>T | ENSP00000389907.2:p.Arg870Trp | |
| ENST00000466819.5:c.86C>T | ||
| ENST00000479614.1:c.86C>T | ||
| ENST00000493220.5:n.2146C>T | ||
| ENST00000495910.6:c.3385C>T | ||
| ENST00000579081.5:c.3712C>T | ENSP00000462408.1:p.Arg1238Trp | |
| NM_000267.3:c.3610C>T , LRG_214t1:c.3610C>T | NP_000258.1:p.Arg1204Trp | |
| NM_001042492.2:c.3610C>T , LRG_214t2:c.3610C>T | NP_001035957.1:p.Arg1204Trp | |
| XM_005257983.1:c.3610C>T | XP_005258040.1:p.Arg1204Trp | |
| XM_005257984.1:c.3610C>T | XP_005258041.1:p.Arg1204Trp | |
| XM_006721922.1:c.3640C>T | XP_006721985.1:p.Arg1214Trp | |
| XM_006721923.2:c.3601C>T | XP_006721986.1:p.Arg1201Trp | |
| XM_006721924.1:c.3640C>T | XP_006721987.1:p.Arg1214Trp | |
| XM_006721925.1:c.3640C>T | XP_006721988.1:p.Arg1214Trp | |
| XM_006721926.2:c.3640C>T | XP_006721989.1:p.Arg1214Trp | |
| XM_006721927.1:c.3640C>T | XP_006721990.1:p.Arg1214Trp | |
| XM_006721928.2:c.3640C>T | XP_006721991.1:p.Arg1214Trp | |
| XM_011524852.1:c.3637C>T | XP_011523154.1:p.Arg1213Trp | |
| XM_011524853.1:c.3601C>T | XP_011523155.1:p.Arg1201Trp | |
| XM_011524854.1:c.3601C>T | XP_011523156.1:p.Arg1201Trp | |
| XM_011524855.1:c.3601C>T | XP_011523157.1:p.Arg1201Trp | |
| XM_011524856.1:c.3601C>T | XP_011523158.1:p.Arg1201Trp | |
| XM_011524857.1:c.3640C>T | XP_011523159.1:p.Arg1214Trp | |
| NM_001042492.3:c.3610C>T MANE Select | NP_001035957.1:p.Arg1204Trp |