Linked Data
ClinVar Variation Id:
469780
dbSNP Id:
rs767473403
ExAC:
5:112174200 G / A
gnomAD v2:
5-112174200-G-A
gnomAD v4:
5-112838503-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112838503G>A , CM000667.2:g.112838503G>A | GRCh38 |
| NC_000005.9:g.112174200G>A , CM000667.1:g.112174200G>A | GRCh37 |
| NC_000005.8:g.112202099G>A | NCBI36 |
| NG_008481.4:g.150983G>A , LRG_130:g.150983G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502371.3:c.2574G>A | ENSP00000484935.2:n.2574G>A | |
| ENST00000504915.3:c.2963G>A | ENSP00000473355.2:p.Ser988Asn | |
| ENST00000505350.2:c.*2915G>A | ENSP00000481752.1:n.*2915G>A | |
| ENST00000507379.6:c.2855G>A | ENSP00000423224.2:p.Ser952Asn | |
| ENST00000509732.6:c.2909G>A | ENSP00000426541.2:p.Ser970Asn | |
| ENST00000512211.7:c.2909G>A | ENSP00000423828.3:p.Ser970Asn | |
| ENST00000257430.9:c.2909G>A MANE Select | ENSP00000257430.4:p.Ser970Asn | |
| ENST00000257430.8:c.2909G>A | ENSP00000257430.4:p.Ser970Asn | |
| ENST00000502371.2:c.1262G>A | ||
| ENST00000507379.5:c.2855G>A | ENSP00000423224.1:p.Ser952Asn | |
| ENST00000508376.6:c.2909G>A | ENSP00000427089.2:p.Ser970Asn | |
| ENST00000508624.5:c.*2231G>A | ENSP00000424265.1:n.*2231G>A | |
| ENST00000512211.6:c.2909G>A | ENSP00000423828.2:p.Ser970Asn | |
| ENST00000520401.1:c.230+9531G>A | ||
| NM_000038.5:c.2909G>A | NP_000029.2:p.Ser970Asn | |
| NM_001127510.2:c.2909G>A | NP_001120982.1:p.Ser970Asn | |
| NM_001127511.2:c.2855G>A | NP_001120983.2:p.Ser952Asn | |
| NM_001354895.1:c.2909G>A | NP_001341824.1:p.Ser970Asn | |
| NM_001354896.1:c.2963G>A | NP_001341825.1:p.Ser988Asn | |
| NM_001354897.1:c.2939G>A | NP_001341826.1:p.Ser980Asn | |
| NM_001354898.1:c.2834G>A | NP_001341827.1:p.Ser945Asn | |
| NM_001354899.1:c.2825G>A | NP_001341828.1:p.Ser942Asn | |
| NM_001354900.1:c.2786G>A | NP_001341829.1:p.Ser929Asn | |
| NM_001354901.1:c.2732G>A | NP_001341830.1:p.Ser911Asn | |
| NM_001354902.1:c.2636G>A | NP_001341831.1:p.Ser879Asn | |
| NM_001354903.1:c.2606G>A | NP_001341832.1:p.Ser869Asn | |
| NM_001354904.1:c.2531G>A | NP_001341833.1:p.Ser844Asn | |
| NM_001354905.1:c.2429G>A | NP_001341834.1:p.Ser810Asn | |
| NM_001354906.1:c.2060G>A | NP_001341835.1:p.Ser687Asn | |
| NM_000038.6:c.2909G>A MANE Select | NP_000029.2:p.Ser970Asn | |
| NM_001127510.3:c.2909G>A | NP_001120982.1:p.Ser970Asn | |
| NM_001127511.3:c.2855G>A | NP_001120983.2:p.Ser952Asn | |
| NM_001354895.2:c.2909G>A | NP_001341824.1:p.Ser970Asn | |
| NM_001354896.2:c.2963G>A | NP_001341825.1:p.Ser988Asn | |
| NM_001354897.2:c.2939G>A | NP_001341826.1:p.Ser980Asn | |
| NM_001354898.2:c.2834G>A | NP_001341827.1:p.Ser945Asn | |
| NM_001354899.2:c.2825G>A | NP_001341828.1:p.Ser942Asn | |
| NM_001354900.2:c.2786G>A | NP_001341829.1:p.Ser929Asn | |
| NM_001354901.2:c.2732G>A | NP_001341830.1:p.Ser911Asn | |
| NM_001354902.2:c.2636G>A | NP_001341831.1:p.Ser879Asn | |
| NM_001354903.2:c.2606G>A | NP_001341832.1:p.Ser869Asn | |
| NM_001354904.2:c.2531G>A | NP_001341833.1:p.Ser844Asn | |
| NM_001354905.2:c.2429G>A | NP_001341834.1:p.Ser810Asn | |
| NM_001354906.2:c.2060G>A | NP_001341835.1:p.Ser687Asn |