Linked Data
ClinVar Variation Id:
449532
dbSNP Id:
rs1555364246
gnomAD v3:
14-50595589-A-G
gnomAD v4:
14-50595589-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.50595589A>G , CM000676.2:g.50595589A>G | GRCh38 |
| NC_000014.8:g.51062307A>G , CM000676.1:g.51062307A>G | GRCh37 |
| NC_000014.7:g.50132057A>G | NCBI36 |
| NG_009028.1:g.67508A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000553509.2:c.587A>G | ENSP00000450989.2:p.Tyr196Cys | |
| ENST00000556478.3:c.587A>G | ENSP00000501428.2:p.Tyr196Cys | |
| ENST00000682037.1:c.587A>G | ENSP00000508289.1:p.Tyr196Cys | |
| ENST00000682219.1:n.1925A>G | ||
| ENST00000682487.1:n.921A>G | ||
| ENST00000683037.1:n.508A>G | ||
| ENST00000683330.1:n.921A>G | ||
| ENST00000683703.1:n.921A>G | ||
| ENST00000683837.1:n.921A>G | ||
| ENST00000358385.12:c.587A>G MANE Select | ENSP00000351155.7:p.Tyr196Cys | |
| ENST00000674288.1:c.*1879A>G | ENSP00000501522.1:n.*1879A>G | |
| ENST00000358385.10:c.587A>G | ENSP00000351155.6:p.Tyr196Cys | |
| ENST00000441560.6:c.587A>G | ENSP00000413675.2:p.Tyr196Cys | |
| ENST00000554886.1:c.155A>G | ENSP00000452074.1:p.Tyr52Cys | |
| NM_001127713.1:c.587A>G | NP_001121185.1:p.Tyr196Cys | |
| NM_015915.4:c.587A>G | NP_056999.2:p.Tyr196Cys | |
| NM_181598.3:c.587A>G | NP_853629.2:p.Tyr196Cys | |
| NM_015915.5:c.587A>G MANE Select | NP_056999.2:p.Tyr196Cys | |
| NM_181598.4:c.587A>G | NP_853629.2:p.Tyr196Cys |