Linked Data
ClinVar Variation Id:
134214
dbSNP Id:
rs76901081
ExAC:
11:44146491 G / A
gnomAD v2:
11-44146491-G-A
gnomAD v3:
11-44124941-G-A
gnomAD v4:
11-44124941-G-A
PubMed:
PMID:24728327
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.44124941G>A , CM000673.2:g.44124941G>A | GRCh38 |
| NC_000011.9:g.44146491G>A , CM000673.1:g.44146491G>A | GRCh37 |
| NC_000011.8:g.44103067G>A | NCBI36 |
| NG_007560.1:g.34393G>A , LRG_494:g.34393G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000343631.4:c.896G>A | ENSP00000342656.3:p.Arg299His | |
| ENST00000395673.8:c.896G>A | ENSP00000379032.4:p.Arg299His | |
| ENST00000531161.6:n.1055G>A | ||
| ENST00000682359.1:c.896G>A | ENSP00000508226.1:p.Arg299His | |
| ENST00000682711.1:c.-544+29089G>A | ENSP00000506803.1:n.-544+29089G>A | |
| ENST00000682815.1:c.896G>A | ENSP00000507234.1:p.Arg299His | |
| ENST00000682947.1:n.1070G>A | ||
| ENST00000682993.1:c.896G>A | ENSP00000507580.1:p.Arg299His | |
| ENST00000683000.1:c.896G>A | ENSP00000508361.1:p.Arg299His | |
| ENST00000683299.1:n.1313G>A | ||
| ENST00000683870.1:c.896G>A | ENSP00000507922.1:p.Arg299His | |
| ENST00000683881.1:n.3457G>A | ||
| ENST00000684039.1:c.896G>A | ENSP00000507677.1:p.Arg299His | |
| ENST00000684124.1:c.896G>A | ENSP00000508332.1:p.Arg299His | |
| ENST00000684533.1:c.744-5104G>A | ENSP00000507915.1:n.744-5104G>A | |
| ENST00000533608.7:c.896G>A MANE Select | ENSP00000431173.2:p.Arg299His | |
| ENST00000343631.3:c.896G>A | ENSP00000342656.3:p.Arg299His | |
| ENST00000358681.8:c.896G>A | ENSP00000351509.4:p.Arg299His | |
| ENST00000395673.7:c.995G>A | ENSP00000379032.3:p.Arg332His | |
| ENST00000531161.5:n.73G>A | ||
| ENST00000533608.5:c.896G>A | ENSP00000431173.1:p.Arg299His | |
| NM_000401.3:c.995G>A , LRG_494t1:c.995G>A | NP_000392.3:p.Arg332His | |
| NM_001178083.1:c.896G>A | NP_001171554.1:p.Arg299His | |
| NM_207122.1:c.896G>A , LRG_494t2:c.896G>A | NP_997005.1:p.Arg299His | |
| XM_011519950.1:c.1034G>A | XP_011518252.1:p.Arg345His | |
| XM_011519951.1:c.935G>A | XP_011518253.1:p.Arg312His | |
| XM_024448383.1:c.1034G>A | XP_024304151.1:p.Arg345His | |
| NM_001178083.2:c.896G>A | NP_001171554.1:p.Arg299His | |
| NM_207122.2:c.896G>A MANE Select | NP_997005.1:p.Arg299His | |
| NM_001178083.3:c.896G>A | NP_001171554.1:p.Arg299His | |
| NM_001389628.1:c.896G>A | NP_001376557.1:p.Arg299His | |
| NM_001389630.1:c.896G>A | NP_001376559.1:p.Arg299His |