Linked Data
ClinVar Variation Id:
134207
dbSNP Id:
rs4755779
ExAC:
11:44129386 A / G
gnomAD v2:
11-44129386-A-G
gnomAD v3:
11-44107836-A-G
gnomAD v4:
11-44107836-A-G
PubMed:
PMID:24728327
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.44107836A>G , CM000673.2:g.44107836A>G | GRCh38 |
| NC_000011.9:g.44129386A>G , CM000673.1:g.44129386A>G | GRCh37 |
| NC_000011.8:g.44085962A>G | NCBI36 |
| NG_007560.1:g.17288A>G , LRG_494:g.17288A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000343631.4:c.124A>G | ENSP00000342656.3:p.Met42Val | |
| ENST00000395673.8:c.124A>G | ENSP00000379032.4:p.Met42Val | |
| ENST00000531161.6:n.283A>G | ||
| ENST00000682359.1:c.124A>G | ENSP00000508226.1:p.Met42Val | |
| ENST00000682711.1:c.-544+11984A>G | ENSP00000506803.1:n.-544+11984A>G | |
| ENST00000682815.1:c.124A>G | ENSP00000507234.1:p.Met42Val | |
| ENST00000682947.1:n.298A>G | ||
| ENST00000682993.1:c.124A>G | ENSP00000507580.1:p.Met42Val | |
| ENST00000683000.1:c.124A>G | ENSP00000508361.1:p.Met42Val | |
| ENST00000683299.1:n.541A>G | ||
| ENST00000683870.1:c.124A>G | ENSP00000507922.1:p.Met42Val | |
| ENST00000683881.1:n.2685A>G | ||
| ENST00000684039.1:c.124A>G | ENSP00000507677.1:p.Met42Val | |
| ENST00000684124.1:c.124A>G | ENSP00000508332.1:p.Met42Val | |
| ENST00000684533.1:c.124A>G | ENSP00000507915.1:p.Met42Val | |
| ENST00000533608.7:c.124A>G MANE Select | ENSP00000431173.2:p.Met42Val | |
| ENST00000343631.3:c.124A>G | ENSP00000342656.3:p.Met42Val | |
| ENST00000358681.8:c.124A>G | ENSP00000351509.4:p.Met42Val | |
| ENST00000395673.7:c.223A>G | ENSP00000379032.3:p.Met75Val | |
| ENST00000527014.1:c.124A>G | ENSP00000434716.1:p.Met42Val | |
| ENST00000532479.1:c.124A>G | ENSP00000433827.1:p.Met42Val | |
| ENST00000533608.5:c.124A>G | ENSP00000431173.1:p.Met42Val | |
| NM_000401.3:c.223A>G , LRG_494t1:c.223A>G | NP_000392.3:p.Met75Val | |
| NM_001178083.1:c.124A>G | NP_001171554.1:p.Met42Val | |
| NM_207122.1:c.124A>G , LRG_494t2:c.124A>G | NP_997005.1:p.Met42Val | |
| XM_011519950.1:c.262A>G | XP_011518252.1:p.Met88Val | |
| XM_011519951.1:c.163A>G | XP_011518253.1:p.Met55Val | |
| XM_024448383.1:c.262A>G | XP_024304151.1:p.Met88Val | |
| NM_001178083.2:c.124A>G | NP_001171554.1:p.Met42Val | |
| NM_207122.2:c.124A>G MANE Select | NP_997005.1:p.Met42Val | |
| NM_001178083.3:c.124A>G | NP_001171554.1:p.Met42Val | |
| NM_001389628.1:c.124A>G | NP_001376557.1:p.Met42Val | |
| NM_001389630.1:c.124A>G | NP_001376559.1:p.Met42Val |