ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.44355852C>G , CM000682.2:g.44355852C>G | GRCh38 |
| NC_000020.10:g.42984492C>G , CM000682.1:g.42984492C>G | GRCh37 |
| NC_000020.9:g.42417906C>G | NCBI36 |
| NG_009818.1:g.5052C>G , LRG_483:g.5052C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000316673.9:c.48C>G MANE Select | ENSP00000315180.4:p.Tyr16Ter | |
| ENST00000316673.8:c.48C>G | ENSP00000315180.4:p.Tyr16Ter | |
| ENST00000457232.5:c.48C>G | ENSP00000396216.1:p.Tyr16Ter | |
| ENST00000609262.5:c.-184C>G | ENSP00000476310.1:n.-184C>G | |
| ENST00000609795.5:c.48C>G | ENSP00000476609.1:p.Tyr16Ter | |
| ENST00000619550.4:c.-184C>G | ENSP00000481331.1:n.-184C>G | |
| NM_001030003.2:c.48C>G | NP_001025174.1:p.Tyr16Ter | |
| NM_001030004.2:c.48C>G | NP_001025175.1:p.Tyr16Ter | |
| NM_001287182.1:c.-184C>G | NP_001274111.1:n.-184C>G | |
| NM_001287183.1:c.-184C>G , LRG_483t3:c.-184C>G | NP_001274112.1:n.-184C>G | |
| NM_001287184.1:c.-184C>G | NP_001274113.1:n.-184C>G | |
| NM_175914.4:c.48C>G , LRG_483t1:c.48C>G | NP_787110.2:p.Tyr16Ter | |
| NM_001030003.3:c.48C>G | NP_001025174.1:p.Tyr16Ter | |
| NM_001030004.3:c.48C>G | NP_001025175.1:p.Tyr16Ter | |
| NM_001287182.2:c.-184C>G | NP_001274111.1:n.-184C>G | |
| NM_001287184.2:c.-184C>G | NP_001274113.1:n.-184C>G | |
| NM_001287183.2:c.-184C>G | NP_001274112.1:n.-184C>G | |
| NM_175914.5:c.48C>G MANE Select | NP_787110.2:p.Tyr16Ter |