Linked Data
ClinVar Variation Id:
310752
dbSNP Id:
rs142528714
ExAC:
12:989017 G / A
gnomAD v2:
12-989017-G-A
gnomAD v3:
12-879851-G-A
gnomAD v4:
12-879851-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.879851G>A , CM000674.2:g.879851G>A | GRCh38 |
| NC_000012.11:g.989017G>A , CM000674.1:g.989017G>A | GRCh37 |
| NC_000012.10:g.859278G>A | NCBI36 |
| NG_007984.2:g.131793G>A | |
| NG_007984.3:g.131793G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000315939.11:c.2652G>A MANE Select | ENSP00000313059.6:p.Ala884= | |
| ENST00000340908.9:c.3867+1490G>A MANE Plus Clinical | ENSP00000341292.5:n.3867+1490G>A | |
| ENST00000674810.1:n.3249G>A | ||
| ENST00000675236.1:n.1547G>A | ||
| ENST00000675631.1:c.1431G>A | ENSP00000502415.1:p.Ala477= | |
| ENST00000676347.1:c.558+1490G>A | ENSP00000501875.1:n.558+1490G>A | |
| ENST00000315939.10:c.2652G>A | ENSP00000313059.6:p.Ala884= | |
| ENST00000340908.8:c.3867+1490G>A | ENSP00000341292.5:n.3867+1490G>A | |
| ENST00000530271.6:c.3891G>A | ENSP00000433548.3:p.Ala1297= | |
| ENST00000535572.5:c.2370+1490G>A | ENSP00000441972.1:n.2370+1490G>A | |
| ENST00000535698.1:c.462G>A | ENSP00000439552.1:p.Ala154= | |
| ENST00000537687.5:c.3613-870G>A | ENSP00000444465.1:n.3613-870G>A | |
| ENST00000542543.1:n.347+1490G>A | ||
| ENST00000544965.5:c.340+1490G>A | ||
| ENST00000545285.5:c.332-870G>A | ||
| NM_001184985.1:c.3613-870G>A | NP_001171914.1:n.3613-870G>A | |
| NM_014823.2:c.2370+1490G>A | NP_055638.2:n.2370+1490G>A | |
| NM_018979.3:c.2652G>A | NP_061852.3:p.Ala884= | |
| NM_213655.4:c.3867+1490G>A | NP_998820.3:n.3867+1490G>A | |
| XM_006719003.1:c.2649G>A | XP_006719066.1:p.Ala883= | |
| XM_011520997.1:c.3891G>A | XP_011519299.1:p.Ala1297= | |
| XM_011520998.1:c.3888G>A | XP_011519300.1:p.Ala1296= | |
| XM_011520999.1:c.3891G>A | XP_011519301.1:p.Ala1297= | |
| XM_011521000.1:c.3891G>A | XP_011519302.1:p.Ala1297= | |
| XM_011521001.1:c.3891G>A | XP_011519303.1:p.Ala1297= | |
| XM_011521002.1:c.3610-870G>A | XP_011519304.1:n.3610-870G>A | |
| XM_011521003.1:c.3612+1490G>A | XP_011519305.1:n.3612+1490G>A | |
| XM_011521004.1:c.3609+1490G>A | XP_011519306.1:n.3609+1490G>A | |
| XM_011521005.1:c.2670G>A | XP_011519307.1:p.Ala890= | |
| XM_011521006.1:c.2568G>A | XP_011519308.1:p.Ala856= | |
| XM_011521007.1:c.2565G>A | XP_011519309.1:p.Ala855= | |
| XM_011521008.1:c.2289+1490G>A | XP_011519310.1:n.2289+1490G>A | |
| XM_011521009.1:c.2286+1490G>A | XP_011519311.1:n.2286+1490G>A | |
| XM_006719003.2:c.2649G>A | XP_006719066.1:p.Ala883= | |
| XM_011520997.3:c.3891G>A | XP_011519299.1:p.Ala1297= | |
| XM_011520998.2:c.3888G>A | XP_011519300.1:p.Ala1296= | |
| XM_011520999.2:c.3891G>A | XP_011519301.1:p.Ala1297= | |
| XM_011521000.2:c.3891G>A | XP_011519302.1:p.Ala1297= | |
| XM_011521001.2:c.3891G>A | XP_011519303.1:p.Ala1297= | |
| XM_011521002.2:c.3610-870G>A | XP_011519304.1:n.3610-870G>A | |
| XM_011521003.2:c.3612+1490G>A | XP_011519305.1:n.3612+1490G>A | |
| XM_011521004.2:c.3609+1490G>A | XP_011519306.1:n.3609+1490G>A | |
| XM_011521005.2:c.2670G>A | XP_011519307.1:p.Ala890= | |
| XM_011521006.2:c.2568G>A | XP_011519308.1:p.Ala856= | |
| XM_011521007.2:c.2565G>A | XP_011519309.1:p.Ala855= | |
| XM_011521008.2:c.2289+1490G>A | XP_011519310.1:n.2289+1490G>A | |
| XM_011521009.2:c.2286+1490G>A | XP_011519311.1:n.2286+1490G>A | |
| XM_017019834.1:c.2371-870G>A | XP_016875323.1:n.2371-870G>A | |
| XM_017019835.1:c.2290-870G>A | XP_016875324.1:n.2290-870G>A | |
| XM_017019836.1:c.2287-870G>A | XP_016875325.1:n.2287-870G>A | |
| XM_017019837.1:c.2373+1490G>A | XP_016875326.1:n.2373+1490G>A | |
| XM_017019838.1:c.2370+1490G>A | XP_016875327.1:n.2370+1490G>A | |
| XM_017019839.1:c.2289+1490G>A | XP_016875328.1:n.2289+1490G>A | |
| NM_018979.4:c.2652G>A MANE Select | NP_061852.3:p.Ala884= | |
| NM_014823.3:c.2370+1490G>A | NP_055638.2:n.2370+1490G>A | |
| NM_001184985.2:c.3613-870G>A | NP_001171914.1:n.3613-870G>A | |
| NM_213655.5:c.3867+1490G>A MANE Plus Clinical | NP_998820.3:n.3867+1490G>A |