Linked Data
ClinVar Variation Id:
469951
ClinVar RCV Id:
RCV000532247
RCV000611032
RCV000573595
RCV002231976
RCV002508225
RCV003403314
RCV003999390
dbSNP Id:
rs1399790840
gnomAD v2:
5-112175391-A-G
gnomAD v3:
5-112839694-A-G
gnomAD v4:
5-112839694-A-G
COSMIC:
COSM1432351
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112839694A>G , CM000667.2:g.112839694A>G | GRCh38 |
| NC_000005.9:g.112175391A>G , CM000667.1:g.112175391A>G | GRCh37 |
| NC_000005.8:g.112203290A>G | NCBI36 |
| NG_008481.4:g.152174A>G , LRG_130:g.152174A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502371.3:c.3765A>G | ENSP00000484935.2:n.3765A>G | |
| ENST00000504915.3:c.4154A>G | ENSP00000473355.2:p.Gln1385Arg | |
| ENST00000505350.2:c.*4106A>G | ENSP00000481752.1:n.*4106A>G | |
| ENST00000507379.6:c.4046A>G | ENSP00000423224.2:p.Gln1349Arg | |
| ENST00000509732.6:c.4100A>G | ENSP00000426541.2:p.Gln1367Arg | |
| ENST00000512211.7:c.4100A>G | ENSP00000423828.3:p.Gln1367Arg | |
| ENST00000257430.9:c.4100A>G MANE Select | ENSP00000257430.4:p.Gln1367Arg | |
| ENST00000257430.8:c.4100A>G | ENSP00000257430.4:p.Gln1367Arg | |
| ENST00000502371.2:c.2453A>G | ||
| ENST00000508376.6:c.4100A>G | ENSP00000427089.2:p.Gln1367Arg | |
| ENST00000508624.5:c.*3422A>G | ENSP00000424265.1:n.*3422A>G | |
| ENST00000520401.1:c.230+10722A>G | ||
| NM_000038.5:c.4100A>G | NP_000029.2:p.Gln1367Arg | |
| NM_001127510.2:c.4100A>G | NP_001120982.1:p.Gln1367Arg | |
| NM_001127511.2:c.4046A>G | NP_001120983.2:p.Gln1349Arg | |
| NM_001354895.1:c.4100A>G | NP_001341824.1:p.Gln1367Arg | |
| NM_001354896.1:c.4154A>G | NP_001341825.1:p.Gln1385Arg | |
| NM_001354897.1:c.4130A>G | NP_001341826.1:p.Gln1377Arg | |
| NM_001354898.1:c.4025A>G | NP_001341827.1:p.Gln1342Arg | |
| NM_001354899.1:c.4016A>G | NP_001341828.1:p.Gln1339Arg | |
| NM_001354900.1:c.3977A>G | NP_001341829.1:p.Gln1326Arg | |
| NM_001354901.1:c.3923A>G | NP_001341830.1:p.Gln1308Arg | |
| NM_001354902.1:c.3827A>G | NP_001341831.1:p.Gln1276Arg | |
| NM_001354903.1:c.3797A>G | NP_001341832.1:p.Gln1266Arg | |
| NM_001354904.1:c.3722A>G | NP_001341833.1:p.Gln1241Arg | |
| NM_001354905.1:c.3620A>G | NP_001341834.1:p.Gln1207Arg | |
| NM_001354906.1:c.3251A>G | NP_001341835.1:p.Gln1084Arg | |
| NM_000038.6:c.4100A>G MANE Select | NP_000029.2:p.Gln1367Arg | |
| NM_001127510.3:c.4100A>G | NP_001120982.1:p.Gln1367Arg | |
| NM_001127511.3:c.4046A>G | NP_001120983.2:p.Gln1349Arg | |
| NM_001354895.2:c.4100A>G | NP_001341824.1:p.Gln1367Arg | |
| NM_001354896.2:c.4154A>G | NP_001341825.1:p.Gln1385Arg | |
| NM_001354897.2:c.4130A>G | NP_001341826.1:p.Gln1377Arg | |
| NM_001354898.2:c.4025A>G | NP_001341827.1:p.Gln1342Arg | |
| NM_001354899.2:c.4016A>G | NP_001341828.1:p.Gln1339Arg | |
| NM_001354900.2:c.3977A>G | NP_001341829.1:p.Gln1326Arg | |
| NM_001354901.2:c.3923A>G | NP_001341830.1:p.Gln1308Arg | |
| NM_001354902.2:c.3827A>G | NP_001341831.1:p.Gln1276Arg | |
| NM_001354903.2:c.3797A>G | NP_001341832.1:p.Gln1266Arg | |
| NM_001354904.2:c.3722A>G | NP_001341833.1:p.Gln1241Arg | |
| NM_001354905.2:c.3620A>G | NP_001341834.1:p.Gln1207Arg | |
| NM_001354906.2:c.3251A>G | NP_001341835.1:p.Gln1084Arg |