Linked Data
ClinVar Variation Id:
235814
ClinVar RCV Id:
RCV000224664
RCV000318559
RCV000695608
RCV000765373
RCV001126448
RCV001126449
RCV004541364
dbSNP Id:
rs202112856
ExAC:
17:56293498 C / T
gnomAD v2:
17-56293498-C-T
gnomAD v3:
17-58216137-C-T
gnomAD v4:
17-58216137-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.58216137C>T , CM000679.2:g.58216137C>T | GRCh38 |
| NC_000017.10:g.56293498C>T , CM000679.1:g.56293498C>T | GRCh37 |
| NC_000017.9:g.53648497C>T | NCBI36 |
| NG_013032.1:g.8469G>A , LRG_687:g.8469G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000313863.11:c.368G>A | ENSP00000316631.6:p.Arg123Gln | |
| ENST00000393119.7:c.368G>A MANE Select | ENSP00000376827.2:p.Arg123Gln | |
| ENST00000537529.7:c.-62G>A | ENSP00000442096.3:n.-62G>A | |
| ENST00000580127.6:c.368G>A | ENSP00000462423.2:p.Arg123Gln | |
| ENST00000581180.2:c.368G>A | ENSP00000502288.1:p.Arg123Gln | |
| ENST00000581761.6:c.368G>A | ENSP00000462129.2:p.Arg123Gln | |
| ENST00000585134.2:c.368G>A | ENSP00000463826.2:p.Arg123Gln | |
| ENST00000675753.2:c.368G>A | ENSP00000502156.1:p.Arg123Gln | |
| ENST00000676787.1:c.368G>A | ENSP00000503999.1:p.Arg123Gln | |
| ENST00000676975.1:c.29G>A | ENSP00000503970.1:p.Arg10Gln | |
| ENST00000677076.1:n.393G>A | ||
| ENST00000677111.1:c.368G>A | ENSP00000504282.1:p.Arg123Gln | |
| ENST00000677160.1:n.393G>A | ||
| ENST00000677416.1:n.393G>A | ||
| ENST00000677475.1:n.396G>A | ||
| ENST00000677486.1:c.261+529G>A | ENSP00000503852.1:n.261+529G>A | |
| ENST00000677546.1:c.368G>A | ENSP00000504043.1:p.Arg123Gln | |
| ENST00000677709.1:n.393G>A | ||
| ENST00000677791.1:n.396G>A | ||
| ENST00000678011.1:n.393G>A | ||
| ENST00000678211.1:n.815G>A | ||
| ENST00000678432.1:c.368G>A | ENSP00000504452.1:p.Arg123Gln | |
| ENST00000678463.1:c.368G>A | ENSP00000502984.1:p.Arg123Gln | |
| ENST00000678481.1:n.396G>A | ||
| ENST00000678568.1:c.191-1299G>A | ENSP00000504754.1:n.191-1299G>A | |
| ENST00000678641.1:c.368G>A | ENSP00000503159.1:p.Arg123Gln | |
| ENST00000678928.1:n.393G>A | ||
| ENST00000679081.1:n.393G>A | ||
| ENST00000313863.10:c.368G>A | ENSP00000316631.6:p.Arg123Gln | |
| ENST00000393119.6:c.368G>A | ENSP00000376827.2:p.Arg123Gln | |
| ENST00000393120.6:c.368G>A | ENSP00000376828.2:p.Arg123Gln | |
| ENST00000537529.6:c.338G>A | ENSP00000442096.2:p.Arg113Gln | |
| ENST00000578789.1:c.*111G>A | ENSP00000462411.1:n.*111G>A | |
| ENST00000580127.5:c.368G>A | ENSP00000462423.1:p.Arg123Gln | |
| ENST00000581180.1:n.368G>A | ||
| ENST00000581761.5:c.191-1299G>A | ENSP00000462129.1:n.191-1299G>A | |
| NM_001165927.1:c.338G>A , LRG_687t2:c.338G>A | NP_001159399.1:p.Arg113Gln | |
| NM_017777.3:c.368G>A , LRG_687t1:c.368G>A | NP_060247.2:p.Arg123Gln | |
| XM_005257483.3:c.368G>A | XP_005257540.1:p.Arg123Gln | |
| XM_005257485.3:c.-122G>A | XP_005257542.1:n.-122G>A | |
| XM_005257486.3:c.-144G>A | XP_005257543.1:n.-144G>A | |
| XM_006721965.2:c.-144G>A | XP_006722028.1:n.-144G>A | |
| XM_011524957.1:c.377G>A | XP_011523259.1:p.Arg126Gln | |
| XM_011524958.1:c.377G>A | XP_011523260.1:p.Arg126Gln | |
| XM_011524959.1:c.377G>A | XP_011523261.1:p.Arg126Gln | |
| XM_011524960.1:c.377G>A | XP_011523262.1:p.Arg126Gln | |
| XR_934494.1:n.425G>A | ||
| NM_001321268.1:c.-144G>A | NP_001308197.1:n.-144G>A | |
| NM_001321269.1:c.368G>A | NP_001308198.1:p.Arg123Gln | |
| NM_001330397.1:c.368G>A | NP_001317326.1:p.Arg123Gln | |
| XM_005257485.4:c.-122G>A | XP_005257542.1:n.-122G>A | |
| XM_006721965.3:c.-144G>A | XP_006722028.1:n.-144G>A | |
| XM_011524957.2:c.377G>A | XP_011523259.1:p.Arg126Gln | |
| XM_011524958.2:c.377G>A | XP_011523260.1:p.Arg126Gln | |
| XM_011524959.2:c.377G>A | XP_011523261.1:p.Arg126Gln | |
| XM_011524960.2:c.377G>A | XP_011523262.1:p.Arg126Gln | |
| XM_017024804.2:c.368G>A | XP_016880293.1:p.Arg123Gln | |
| XM_017024805.1:c.-122G>A | XP_016880294.1:n.-122G>A | |
| XR_002958042.1:n.422G>A | ||
| NM_001321268.2:c.-144G>A | NP_001308197.1:n.-144G>A | |
| NM_001321269.2:c.368G>A | NP_001308198.1:p.Arg123Gln | |
| NM_001330397.2:c.368G>A | NP_001317326.1:p.Arg123Gln | |
| NM_017777.4:c.368G>A MANE Select | NP_060247.2:p.Arg123Gln |