Linked Data
ClinVar Variation Id:
217924
ClinVar RCV Id:
RCV000202161
RCV000204247
RCV000490831
RCV000763540
RCV003422107
RCV003987449
RCV003997041
RCV000500343
dbSNP Id:
rs863225311
COSMIC:
COSM3768903
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112819347A>G , CM000667.2:g.112819347A>G | GRCh38 |
| NC_000005.9:g.112155044A>G , CM000667.1:g.112155044A>G | GRCh37 |
| NC_000005.8:g.112182943A>G | NCBI36 |
| NG_008481.4:g.131827A>G , LRG_130:g.131827A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502371.3:c.1312+3A>G | ENSP00000484935.2:n.1312+3A>G | |
| ENST00000504915.3:c.1312+3A>G | ENSP00000473355.2:n.1312+3A>G | |
| ENST00000505084.2:n.1368+3A>G | ||
| ENST00000505350.2:c.*1318+3A>G | ENSP00000481752.1:n.*1318+3A>G | |
| ENST00000507379.6:c.1258+3A>G | ENSP00000423224.2:n.1258+3A>G | |
| ENST00000509732.6:c.1312+3A>G | ENSP00000426541.2:n.1312+3A>G | |
| ENST00000512211.7:c.1312+3A>G | ENSP00000423828.3:n.1312+3A>G | |
| ENST00000257430.9:c.1312+3A>G MANE Select | ENSP00000257430.4:n.1312+3A>G | |
| ENST00000257430.8:c.1312+3A>G | ENSP00000257430.4:n.1312+3A>G | |
| ENST00000507379.5:c.1258+3A>G | ENSP00000423224.1:n.1258+3A>G | |
| ENST00000508376.6:c.1312+3A>G | ENSP00000427089.2:n.1312+3A>G | |
| ENST00000508624.5:c.*634+3A>G | ENSP00000424265.1:n.*634+3A>G | |
| ENST00000512211.6:c.1312+3A>G | ENSP00000423828.2:n.1312+3A>G | |
| NM_000038.5:c.1312+3A>G | NP_000029.2:n.1312+3A>G | |
| NM_001127510.2:c.1312+3A>G | NP_001120982.1:n.1312+3A>G | |
| NM_001127511.2:c.1258+3A>G | NP_001120983.2:n.1258+3A>G | |
| NM_001354895.1:c.1312+3A>G | NP_001341824.1:n.1312+3A>G | |
| NM_001354896.1:c.1312+3A>G | NP_001341825.1:n.1312+3A>G | |
| NM_001354897.1:c.1342+3A>G | NP_001341826.1:n.1342+3A>G | |
| NM_001354898.1:c.1237+3A>G | NP_001341827.1:n.1237+3A>G | |
| NM_001354899.1:c.1228+3A>G | NP_001341828.1:n.1228+3A>G | |
| NM_001354900.1:c.1135+3A>G | NP_001341829.1:n.1135+3A>G | |
| NM_001354901.1:c.1135+3A>G | NP_001341830.1:n.1135+3A>G | |
| NM_001354902.1:c.1039+3A>G | NP_001341831.1:n.1039+3A>G | |
| NM_001354903.1:c.1009+3A>G | NP_001341832.1:n.1009+3A>G | |
| NM_001354904.1:c.934+3A>G | NP_001341833.1:n.934+3A>G | |
| NM_001354905.1:c.832+3A>G | NP_001341834.1:n.832+3A>G | |
| NM_001354906.1:c.463+3A>G | NP_001341835.1:n.463+3A>G | |
| NM_000038.6:c.1312+3A>G MANE Select | NP_000029.2:n.1312+3A>G | |
| NM_001127510.3:c.1312+3A>G | NP_001120982.1:n.1312+3A>G | |
| NM_001127511.3:c.1258+3A>G | NP_001120983.2:n.1258+3A>G | |
| NM_001354895.2:c.1312+3A>G | NP_001341824.1:n.1312+3A>G | |
| NM_001354896.2:c.1312+3A>G | NP_001341825.1:n.1312+3A>G | |
| NM_001354897.2:c.1342+3A>G | NP_001341826.1:n.1342+3A>G | |
| NM_001354898.2:c.1237+3A>G | NP_001341827.1:n.1237+3A>G | |
| NM_001354899.2:c.1228+3A>G | NP_001341828.1:n.1228+3A>G | |
| NM_001354900.2:c.1135+3A>G | NP_001341829.1:n.1135+3A>G | |
| NM_001354901.2:c.1135+3A>G | NP_001341830.1:n.1135+3A>G | |
| NM_001354902.2:c.1039+3A>G | NP_001341831.1:n.1039+3A>G | |
| NM_001354903.2:c.1009+3A>G | NP_001341832.1:n.1009+3A>G | |
| NM_001354904.2:c.934+3A>G | NP_001341833.1:n.934+3A>G | |
| NM_001354905.2:c.832+3A>G | NP_001341834.1:n.832+3A>G | |
| NM_001354906.2:c.463+3A>G | NP_001341835.1:n.463+3A>G |