Linked Data
ClinVar Variation Id:
8466
dbSNP Id:
rs267606621
gnomAD v4:
16-70268356-C-T
COSMIC:
COSM4062311
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.70268356C>T , CM000678.2:g.70268356C>T | GRCh38 |
| NC_000016.9:g.70302259C>T , CM000678.1:g.70302259C>T | GRCh37 |
| NC_000016.8:g.68859760C>T | NCBI36 |
| NG_023191.1:g.26154G>A , LRG_359:g.26154G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000261772.13:c.986G>A MANE Select | ENSP00000261772.8:p.Arg329His | |
| ENST00000564359.6:n.1144G>A | ||
| ENST00000565361.3:c.986G>A | ENSP00000455360.3:p.Arg329His | |
| ENST00000674512.1:c.986G>A | ENSP00000501613.1:p.Arg329His | |
| ENST00000674652.1:c.*13G>A | ENSP00000502620.1:n.*13G>A | |
| ENST00000674691.1:c.986G>A | ENSP00000502247.1:p.Arg329His | |
| ENST00000674768.1:c.986G>A | ENSP00000501679.1:p.Arg329His | |
| ENST00000674811.1:c.962+1262G>A | ENSP00000502055.1:n.962+1262G>A | |
| ENST00000674848.1:n.1035G>A | ||
| ENST00000674962.1:n.1144G>A | ||
| ENST00000674963.1:c.986G>A | ENSP00000501924.1:p.Arg329His | |
| ENST00000675035.1:c.986G>A | ENSP00000502712.1:p.Arg329His | |
| ENST00000675045.1:c.986G>A | ENSP00000502014.1:p.Arg329His | |
| ENST00000675120.1:c.986G>A | ENSP00000502823.1:p.Arg329His | |
| ENST00000675133.1:c.986G>A | ENSP00000502230.1:p.Arg329His | |
| ENST00000675270.1:n.1121G>A | ||
| ENST00000675297.1:c.986G>A | ENSP00000502753.1:p.Arg329His | |
| ENST00000675338.1:n.1142G>A | ||
| ENST00000675371.1:c.986G>A | ENSP00000502645.1:p.Arg329His | |
| ENST00000675403.1:n.1144G>A | ||
| ENST00000675569.1:c.*220G>A | ENSP00000502534.1:n.*220G>A | |
| ENST00000675643.1:c.986G>A | ENSP00000502797.1:p.Arg329His | |
| ENST00000675691.1:c.857G>A | ENSP00000502196.1:p.Arg286His | |
| ENST00000675751.1:c.*13G>A | ENSP00000502277.1:n.*13G>A | |
| ENST00000675853.1:c.986G>A | ENSP00000502367.1:p.Arg329His | |
| ENST00000675917.1:n.1283G>A | ||
| ENST00000675953.1:c.902G>A | ENSP00000502321.1:p.Arg301His | |
| ENST00000675986.1:n.1144G>A | ||
| ENST00000676004.1:c.*985G>A | ENSP00000502765.1:n.*985G>A | |
| ENST00000676040.1:c.*220G>A | ENSP00000502108.1:n.*220G>A | |
| ENST00000676168.1:c.986G>A | ENSP00000502479.1:p.Arg329His | |
| ENST00000676209.1:c.986G>A | ENSP00000502052.1:p.Arg329His | |
| ENST00000676211.1:c.*13G>A | ENSP00000502726.1:n.*13G>A | |
| ENST00000676212.1:c.986G>A | ENSP00000501853.1:p.Arg329His | |
| ENST00000676247.1:c.986G>A | ENSP00000502699.1:p.Arg329His | |
| ENST00000261772.12:c.986G>A | ENSP00000261772.7:p.Arg329His | |
| NM_001605.2:c.986G>A , LRG_359t1:c.986G>A | NP_001596.2:p.Arg329His | |
| XR_933220.1:n.1137G>A | ||
| XR_933220.3:n.1096G>A | ||
| NM_001605.3:c.986G>A MANE Select | NP_001596.2:p.Arg329His |