Linked Data
ClinVar Variation Id:
231010
dbSNP Id:
rs142316409
ExAC:
17:33428014 C / T
gnomAD v2:
17-33428014-C-T
gnomAD v3:
17-35100995-C-T
gnomAD v4:
17-35100995-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.35100995C>T , CM000679.2:g.35100995C>T | GRCh38 |
| NC_000017.10:g.33428014C>T , CM000679.1:g.33428014C>T | GRCh37 |
| NC_000017.9:g.30452127C>T | NCBI36 |
| NG_031858.1:g.23875G>A , LRG_516:g.23875G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000586186.3:c.810G>A | ENSP00000468273.3:p.Gly270= | |
| ENST00000587405.6:c.588G>A | ENSP00000466478.2:p.Gly196= | |
| ENST00000590016.6:c.1005G>A | ENSP00000466399.1:p.Gly335= | |
| ENST00000592577.6:c.588G>A | ENSP00000466839.2:p.Gly196= | |
| ENST00000345365.11:c.945G>A MANE Select | ENSP00000338790.6:p.Gly315= | |
| ENST00000335858.11:c.609G>A | ENSP00000338408.6:p.Gly203= | |
| ENST00000345365.10:c.945G>A | ENSP00000338790.6:p.Gly315= | |
| ENST00000394589.8:c.945G>A | ENSP00000378090.4:p.Gly315= | |
| ENST00000460118.6:c.414G>A | ENSP00000464356.2:p.Gly138= | |
| ENST00000586044.5:c.*676G>A | ENSP00000465584.1:n.*676G>A | |
| ENST00000586210.5:c.*539G>A | ENSP00000465612.1:n.*539G>A | |
| ENST00000587977.5:c.*685G>A | ENSP00000466587.1:n.*685G>A | |
| ENST00000588372.5:c.*428G>A | ENSP00000468764.1:n.*428G>A | |
| ENST00000588594.5:c.*541G>A | ENSP00000465366.1:n.*541G>A | |
| ENST00000590016.5:c.1005G>A | ENSP00000466399.1:p.Gly335= | |
| ENST00000591723.5:c.372+206G>A | ENSP00000467986.1:n.372+206G>A | |
| ENST00000592181.1:c.546+206G>A | ENSP00000464799.1:n.546+206G>A | |
| ENST00000593039.5:c.426+206G>A | ENSP00000466834.1:n.426+206G>A | |
| NM_001142571.1:c.1005G>A | NP_001136043.1:p.Gly335= | |
| NM_002878.3:c.945G>A , LRG_516t1:c.945G>A | NP_002869.3:p.Gly315= | |
| NM_133629.2:c.609G>A | NP_598332.1:p.Gly203= | |
| NR_037711.1:n.1082G>A | ||
| NR_037712.1:n.947G>A | ||
| NR_037714.1:n.655+206G>A | ||
| NM_001142571.2:c.1005G>A | NP_001136043.1:p.Gly335= | |
| NM_133629.3:c.609G>A | NP_598332.1:p.Gly203= | |
| NR_037711.2:n.971G>A | ||
| NR_037712.2:n.836G>A | ||
| NM_002878.4:c.945G>A MANE Select | NP_002869.3:p.Gly315= |