Linked Data
dbSNP Id:
rs781080546
ExAC:
8:61773632 A / C
gnomAD v2:
8-61773632-A-C
gnomAD v4:
8-60861073-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.60861073A>C , CM000670.2:g.60861073A>C | GRCh38 |
| NC_000008.10:g.61773632A>C , CM000670.1:g.61773632A>C | GRCh37 |
| NC_000008.9:g.61936186A>C | NCBI36 |
| NG_007009.1:g.187294A>C , LRG_176:g.187294A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695850.1:n.954A>C | ||
| ENST00000695851.1:n.158A>C | ||
| ENST00000695853.1:c.*837A>C | ENSP00000512218.1:n.*837A>C | |
| ENST00000423902.7:c.7778A>C MANE Select | ENSP00000392028.1:p.Glu2593Ala | |
| ENST00000423902.6:c.7778A>C | ENSP00000392028.1:p.Glu2593Ala | |
| ENST00000524602.5:c.1717-1156A>C | ENSP00000437061.1:n.1717-1156A>C | |
| ENST00000531695.1:n.202A>C | ||
| ENST00000618450.1:n.170A>C | ||
| NM_001316690.1:c.1717-1156A>C | NP_001303619.1:n.1717-1156A>C | |
| NM_017780.3:c.7778A>C | NP_060250.2:p.Glu2593Ala | |
| XM_011517553.1:c.7868A>C | XP_011515855.1:p.Glu2623Ala | |
| XM_011517554.1:c.7868A>C | XP_011515856.1:p.Glu2623Ala | |
| XM_011517555.1:c.7865A>C | XP_011515857.1:p.Glu2622Ala | |
| XM_011517556.1:c.7699-1123A>C | XP_011515858.1:n.7699-1123A>C | |
| XM_011517557.1:c.5855A>C | XP_011515859.1:p.Glu1952Ala | |
| XM_011517558.1:c.5405A>C | XP_011515860.1:p.Glu1802Ala | |
| XM_011517559.1:c.4613A>C | XP_011515861.1:p.Glu1538Ala | |
| XM_011517553.2:c.7868A>C | XP_011515855.1:p.Glu2623Ala | |
| XM_011517554.3:c.7868A>C | XP_011515856.1:p.Glu2623Ala | |
| XM_011517555.2:c.7865A>C | XP_011515857.1:p.Glu2622Ala | |
| XM_017013612.1:c.7868A>C | XP_016869101.1:p.Glu2623Ala | |
| XM_017013613.1:c.7775A>C | XP_016869102.1:p.Glu2592Ala | |
| NM_017780.4:c.7778A>C MANE Select | NP_060250.2:p.Glu2593Ala |