Linked Data
dbSNP Id:
rs774920311
ExAC:
4:69535860 C / T
gnomAD v2:
4-69535860-C-T
gnomAD v4:
4-68670142-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.68670142C>T , CM000666.2:g.68670142C>T | GRCh38 |
| NC_000004.11:g.69535860C>T , CM000666.1:g.69535860C>T | GRCh37 |
| NC_000004.10:g.69218455C>T | NCBI36 |
| NG_052676.1:g.5635G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000338206.6:c.477G>A MANE Select | ENSP00000341045.5:p.Glu159= | |
| ENST00000338206.5:c.477G>A | ENSP00000341045.5:p.Glu159= | |
| ENST00000616841.4:c.477G>A | ENSP00000482004.1:p.Glu159= | |
| NM_001076.3:c.477G>A | NP_001067.2:p.Glu159= | |
| NM_001076.4:c.477G>A MANE Select | NP_001067.2:p.Glu159= |