Linked Data
ClinVar Variation Id:
1778193
dbSNP Id:
rs753915461
gnomAD v2:
16-3294505-T-C
gnomAD v4:
16-3244505-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.3244505T>C , CM000678.2:g.3244505T>C | GRCh38 |
| NC_000016.9:g.3294505T>C , CM000678.1:g.3294505T>C | GRCh37 |
| NC_000016.8:g.3234506T>C | NCBI36 |
| NG_007871.1:g.17123A>G , LRG_190:g.17123A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000697124.1:n.815A>G | ||
| ENST00000219596.6:c.1694A>G MANE Select | ENSP00000219596.1:p.Glu565Gly | |
| ENST00000219596.5:c.1694A>G | ENSP00000219596.1:p.Glu565Gly | |
| ENST00000339854.8:c.1154A>G | ENSP00000339639.4:p.Glu385Gly | |
| ENST00000536379.5:c.1061A>G | ENSP00000445079.1:p.Glu354Gly | |
| ENST00000536980.5:c.1061A>G | ENSP00000444178.1:p.Glu354Gly | |
| ENST00000537682.5:c.1694A>G | ENSP00000438611.1:p.Glu565Gly | |
| ENST00000538326.5:c.*319A>G | ENSP00000437486.1:n.*319A>G | |
| ENST00000539145.5:c.615A>G | ENSP00000444471.1:n.615A>G | |
| ENST00000541159.5:c.1061A>G | ENSP00000438711.1:p.Glu354Gly | |
| ENST00000542898.5:c.1787A>G | ENSP00000444615.1:p.Glu596Gly | |
| ENST00000570511.5:c.1165-613A>G | ENSP00000458312.1:n.1165-613A>G | |
| ENST00000572244.5:c.384A>G | ENSP00000461186.1:n.384A>G | |
| ENST00000574583.5:c.532-613A>G | ENSP00000460269.1:n.532-613A>G | |
| ENST00000576315.5:c.532-219A>G | ENSP00000460551.1:n.532-219A>G | |
| ENST00000621655.1:c.1061A>G | ENSP00000481436.1:p.Glu354Gly | |
| NM_000243.2:c.1694A>G , LRG_190t1:c.1694A>G | NP_000234.1:p.Glu565Gly | |
| NM_001198536.1:c.1061A>G | NP_001185465.1:p.Glu354Gly | |
| XM_017023236.2:c.1691A>G | XP_016878725.1:p.Glu564Gly | |
| XR_001751903.1:n.1883A>G | ||
| NM_000243.3:c.1694A>G MANE Select | NP_000234.1:p.Glu565Gly | |
| NM_001198536.2:c.1061A>G | NP_001185465.2:p.Glu354Gly |