Linked Data
ClinVar Variation Id:
219832
dbSNP Id:
rs774605759
ExAC:
17:59760976 T / C
gnomAD v2:
17-59760976-T-C
gnomAD v3:
17-61683615-T-C
gnomAD v4:
17-61683615-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.61683615T>C , CM000679.2:g.61683615T>C | GRCh38 |
| NC_000017.10:g.59760976T>C , CM000679.1:g.59760976T>C | GRCh37 |
| NC_000017.9:g.57115758T>C | NCBI36 |
| NG_007409.2:g.184945A>G , LRG_300:g.184945A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682073.1:n.2171A>G | ||
| ENST00000682453.1:c.3431A>G | ENSP00000506943.1:p.Glu1144Gly | |
| ENST00000682477.1:c.*2857A>G | ENSP00000507075.1:n.*2857A>G | |
| ENST00000682589.1:n.9308A>G | ||
| ENST00000682755.1:c.3209A>G | ENSP00000507660.1:p.Glu1070Gly | |
| ENST00000682989.1:c.*522A>G | ENSP00000507786.1:n.*522A>G | |
| ENST00000683039.1:c.3431A>G | ENSP00000508303.1:p.Glu1144Gly | |
| ENST00000683235.1:c.*846A>G | ENSP00000507646.1:n.*846A>G | |
| ENST00000683535.1:n.1561A>G | ||
| ENST00000684584.1:c.2594A>G | ENSP00000508044.1:p.Glu865Gly | |
| ENST00000684626.1:n.1677A>G | ||
| ENST00000684769.1:c.1621A>G | ENSP00000507691.1:n.1621A>G | |
| ENST00000259008.7:c.3431A>G MANE Select | ENSP00000259008.2:p.Glu1144Gly | |
| ENST00000259008.6:c.3431A>G | ENSP00000259008.2:p.Glu1144Gly | |
| NM_032043.2:c.3431A>G , LRG_300t1:c.3431A>G | NP_114432.2:p.Glu1144Gly | |
| XM_011525332.1:c.3491A>G | XP_011523634.1:p.Glu1164Gly | |
| XM_011525333.1:c.3491A>G | XP_011523635.1:p.Glu1164Gly | |
| XM_011525334.1:c.3491A>G | XP_011523636.1:p.Glu1164Gly | |
| XM_011525335.1:c.3431A>G | XP_011523637.1:p.Glu1144Gly | |
| XM_011525336.1:c.3371A>G | XP_011523638.1:p.Glu1124Gly | |
| XM_011525337.1:c.3290A>G | XP_011523639.1:p.Glu1097Gly | |
| XM_011525338.1:c.3008A>G | XP_011523640.1:p.Glu1003Gly | |
| XM_011525332.3:c.3491A>G | XP_011523634.1:p.Glu1164Gly | |
| XM_011525333.3:c.3491A>G | XP_011523635.1:p.Glu1164Gly | |
| XM_011525334.2:c.3491A>G | XP_011523636.1:p.Glu1164Gly | |
| XM_011525335.3:c.3431A>G | XP_011523637.1:p.Glu1144Gly | |
| XM_011525336.2:c.3371A>G | XP_011523638.1:p.Glu1124Gly | |
| XM_011525337.2:c.3290A>G | XP_011523639.1:p.Glu1097Gly | |
| XM_011525338.2:c.3008A>G | XP_011523640.1:p.Glu1003Gly | |
| XM_017025200.1:c.2948A>G | XP_016880689.1:p.Glu983Gly | |
| XM_017025201.1:c.2948A>G | XP_016880690.1:p.Glu983Gly | |
| XM_017025202.1:c.1577A>G | XP_016880691.1:p.Glu526Gly | |
| XM_017025203.1:c.1577A>G | XP_016880692.1:p.Glu526Gly | |
| NM_032043.3:c.3431A>G MANE Select | NP_114432.2:p.Glu1144Gly |