Linked Data
ClinVar Variation Id:
216156
dbSNP Id:
rs762990578
ExAC:
5:112173735 A / C
gnomAD v2:
5-112173735-A-C
gnomAD v3:
5-112838038-A-C
gnomAD v4:
5-112838038-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112838038A>C , CM000667.2:g.112838038A>C | GRCh38 |
| NC_000005.9:g.112173735A>C , CM000667.1:g.112173735A>C | GRCh37 |
| NC_000005.8:g.112201634A>C | NCBI36 |
| NG_008481.4:g.150518A>C , LRG_130:g.150518A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502371.3:c.2109A>C | ENSP00000484935.2:n.2109A>C | |
| ENST00000504915.3:c.2498A>C | ENSP00000473355.2:p.Asn833Thr | |
| ENST00000505350.2:c.*2450A>C | ENSP00000481752.1:n.*2450A>C | |
| ENST00000507379.6:c.2390A>C | ENSP00000423224.2:p.Asn797Thr | |
| ENST00000509732.6:c.2444A>C | ENSP00000426541.2:p.Asn815Thr | |
| ENST00000512211.7:c.2444A>C | ENSP00000423828.3:p.Asn815Thr | |
| ENST00000257430.9:c.2444A>C MANE Select | ENSP00000257430.4:p.Asn815Thr | |
| ENST00000257430.8:c.2444A>C | ENSP00000257430.4:p.Asn815Thr | |
| ENST00000502371.2:c.797A>C | ||
| ENST00000507379.5:c.2390A>C | ENSP00000423224.1:p.Asn797Thr | |
| ENST00000508376.6:c.2444A>C | ENSP00000427089.2:p.Asn815Thr | |
| ENST00000508624.5:c.*1766A>C | ENSP00000424265.1:n.*1766A>C | |
| ENST00000512211.6:c.2444A>C | ENSP00000423828.2:p.Asn815Thr | |
| ENST00000520401.1:c.230+9066A>C | ||
| NM_000038.5:c.2444A>C | NP_000029.2:p.Asn815Thr | |
| NM_001127510.2:c.2444A>C | NP_001120982.1:p.Asn815Thr | |
| NM_001127511.2:c.2390A>C | NP_001120983.2:p.Asn797Thr | |
| NM_001354895.1:c.2444A>C | NP_001341824.1:p.Asn815Thr | |
| NM_001354896.1:c.2498A>C | NP_001341825.1:p.Asn833Thr | |
| NM_001354897.1:c.2474A>C | NP_001341826.1:p.Asn825Thr | |
| NM_001354898.1:c.2369A>C | NP_001341827.1:p.Asn790Thr | |
| NM_001354899.1:c.2360A>C | NP_001341828.1:p.Asn787Thr | |
| NM_001354900.1:c.2321A>C | NP_001341829.1:p.Asn774Thr | |
| NM_001354901.1:c.2267A>C | NP_001341830.1:p.Asn756Thr | |
| NM_001354902.1:c.2171A>C | NP_001341831.1:p.Asn724Thr | |
| NM_001354903.1:c.2141A>C | NP_001341832.1:p.Asn714Thr | |
| NM_001354904.1:c.2066A>C | NP_001341833.1:p.Asn689Thr | |
| NM_001354905.1:c.1964A>C | NP_001341834.1:p.Asn655Thr | |
| NM_001354906.1:c.1595A>C | NP_001341835.1:p.Asn532Thr | |
| NM_000038.6:c.2444A>C MANE Select | NP_000029.2:p.Asn815Thr | |
| NM_001127510.3:c.2444A>C | NP_001120982.1:p.Asn815Thr | |
| NM_001127511.3:c.2390A>C | NP_001120983.2:p.Asn797Thr | |
| NM_001354895.2:c.2444A>C | NP_001341824.1:p.Asn815Thr | |
| NM_001354896.2:c.2498A>C | NP_001341825.1:p.Asn833Thr | |
| NM_001354897.2:c.2474A>C | NP_001341826.1:p.Asn825Thr | |
| NM_001354898.2:c.2369A>C | NP_001341827.1:p.Asn790Thr | |
| NM_001354899.2:c.2360A>C | NP_001341828.1:p.Asn787Thr | |
| NM_001354900.2:c.2321A>C | NP_001341829.1:p.Asn774Thr | |
| NM_001354901.2:c.2267A>C | NP_001341830.1:p.Asn756Thr | |
| NM_001354902.2:c.2171A>C | NP_001341831.1:p.Asn724Thr | |
| NM_001354903.2:c.2141A>C | NP_001341832.1:p.Asn714Thr | |
| NM_001354904.2:c.2066A>C | NP_001341833.1:p.Asn689Thr | |
| NM_001354905.2:c.1964A>C | NP_001341834.1:p.Asn655Thr | |
| NM_001354906.2:c.1595A>C | NP_001341835.1:p.Asn532Thr |