Linked Data
ClinVar Variation Id:
9216
ClinVar RCV Id:
RCV000009796
dbSNP Id:
rs137853338
PubMed:
PMID:17407387
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.44424243T>G , CM000682.2:g.44424243T>G | GRCh38 |
| NC_000020.10:g.43052883T>G , CM000682.1:g.43052883T>G | GRCh37 |
| NC_000020.9:g.42486297T>G | NCBI36 |
| NG_009818.1:g.73443T>G , LRG_483:g.73443T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000316673.9:c.1052T>G MANE Select | ENSP00000315180.4:p.Met351Arg | |
| ENST00000316099.10:c.1118T>G | ENSP00000312987.3:p.Met373Arg | |
| ENST00000619550.5:c.1092T>G | ||
| ENST00000316099.9:c.1118T>G | ENSP00000312987.3:p.Met373Arg | |
| ENST00000316099.8:c.1118T>G | ENSP00000312987.3:p.Met373Arg | |
| ENST00000316673.8:c.1052T>G | ENSP00000315180.4:p.Met351Arg | |
| ENST00000372920.1:c.*885T>G | ENSP00000362011.1:n.*885T>G | |
| ENST00000415691.2:c.1118T>G | ENSP00000412111.1:p.Met373Arg | |
| ENST00000443598.6:c.1118T>G | ENSP00000410911.2:p.Met373Arg | |
| ENST00000457232.5:c.1052T>G | ENSP00000396216.1:p.Met351Arg | |
| ENST00000609795.5:c.1052T>G | ENSP00000476609.1:p.Met351Arg | |
| ENST00000619550.4:c.1043T>G | ENSP00000481331.1:p.Met348Arg | |
| NM_000457.4:c.1118T>G , LRG_483t2:c.1118T>G | NP_000448.3:p.Met373Arg | |
| NM_001030003.2:c.1052T>G | NP_001025174.1:p.Met351Arg | |
| NM_001030004.2:c.1052T>G | NP_001025175.1:p.Met351Arg | |
| NM_001258355.1:c.1097T>G | NP_001245284.1:p.Met366Arg | |
| NM_001287182.1:c.1043T>G | NP_001274111.1:p.Met348Arg | |
| NM_001287183.1:c.1043T>G , LRG_483t3:c.1043T>G | NP_001274112.1:p.Met348Arg | |
| NM_001287184.1:c.1043T>G | NP_001274113.1:p.Met348Arg | |
| NM_175914.4:c.1052T>G , LRG_483t1:c.1052T>G | NP_787110.2:p.Met351Arg | |
| NM_178849.2:c.1118T>G | NP_849180.1:p.Met373Arg | |
| NM_178850.2:c.1118T>G | NP_849181.1:p.Met373Arg | |
| XM_005260407.2:c.1235T>G | XP_005260464.1:p.Met412Arg | |
| XM_011528797.1:c.1166T>G | XP_011527099.1:p.Met389Arg | |
| XM_011528798.1:c.1166T>G | XP_011527100.1:p.Met389Arg | |
| XM_005260407.4:c.1235T>G | XP_005260464.1:p.Met412Arg | |
| NM_001030003.3:c.1052T>G | NP_001025174.1:p.Met351Arg | |
| NM_001030004.3:c.1052T>G | NP_001025175.1:p.Met351Arg | |
| NM_001258355.2:c.1097T>G | NP_001245284.1:p.Met366Arg | |
| NM_001287182.2:c.1043T>G | NP_001274111.1:p.Met348Arg | |
| NM_001287184.2:c.1043T>G | NP_001274113.1:p.Met348Arg | |
| NM_178849.3:c.1118T>G | NP_849180.1:p.Met373Arg | |
| NM_178850.3:c.1118T>G | NP_849181.1:p.Met373Arg | |
| NM_000457.5:c.1118T>G | NP_000448.3:p.Met373Arg | |
| NM_000457.6:c.1118T>G | NP_000448.3:p.Met373Arg | |
| NM_001287183.2:c.1043T>G | NP_001274112.1:p.Met348Arg | |
| NM_175914.5:c.1052T>G MANE Select | NP_787110.2:p.Met351Arg |