Linked Data
ClinVar Variation Id:
21272
dbSNP Id:
rs80338862
ExAC:
11:71146621 C / T
gnomAD v2:
11-71146621-C-T
gnomAD v3:
11-71435575-C-T
gnomAD v4:
11-71435575-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.71435575C>T , CM000673.2:g.71435575C>T | GRCh38 |
| NC_000011.9:g.71146621C>T , CM000673.1:g.71146621C>T | GRCh37 |
| NC_000011.8:g.70824269C>T | NCBI36 |
| NG_012655.2:g.17857G>A , LRG_340:g.17857G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000525346.6:c.1228G>A | ENSP00000435707.3:p.Gly410Ser | |
| ENST00000526780.6:c.1228G>A | ENSP00000435668.2:p.Gly410Ser | |
| ENST00000527316.6:c.1054G>A | ENSP00000435047.2:p.Gly352Ser | |
| ENST00000682708.1:c.1279G>A | ENSP00000506866.1:p.Gly427Ser | |
| ENST00000683287.1:c.1264G>A | ENSP00000507607.1:p.Gly422Ser | |
| ENST00000683714.1:c.1236G>A | ENSP00000508207.1:p.Ser412= | |
| ENST00000684396.1:n.1268G>A | ||
| ENST00000685320.1:c.643G>A | ENSP00000509319.1:p.Gly215Ser | |
| ENST00000690257.1:c.1132G>A | ENSP00000510750.1:p.Gly378Ser | |
| ENST00000355527.8:c.1228G>A MANE Select | ENSP00000347717.4:p.Gly410Ser | |
| ENST00000355527.7:c.1228G>A | ENSP00000347717.3:p.Gly410Ser | |
| ENST00000407721.6:c.1228G>A | ENSP00000384739.2:p.Gly410Ser | |
| ENST00000525137.1:c.729G>A | ENSP00000435956.1:p.Ser243= | |
| ENST00000533800.5:c.478G>A | ENSP00000435011.1:p.Gly160Ser | |
| ENST00000534795.5:c.319+2237G>A | ||
| NM_001163817.1:c.1228G>A | NP_001157289.1:p.Gly410Ser | |
| NM_001360.2:c.1228G>A , LRG_340t1:c.1228G>A | NP_001351.2:p.Gly410Ser | |
| XM_011544777.1:c.1362G>A | XP_011543079.1:p.Ser454= | |
| XM_011544777.2:c.1362G>A | XP_011543079.1:p.Ser454= | |
| NM_001163817.2:c.1228G>A | NP_001157289.1:p.Gly410Ser | |
| NM_001360.3:c.1228G>A MANE Select | NP_001351.2:p.Gly410Ser |