Linked Data
ClinVar Variation Id:
287293
dbSNP Id:
rs145102275
ExAC:
6:66044979 A / T
gnomAD v2:
6-66044979-A-T
gnomAD v3:
6-65335086-A-T
gnomAD v4:
6-65335086-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.65335086A>T , CM000668.2:g.65335086A>T | GRCh38 |
| NC_000006.11:g.66044979A>T , CM000668.1:g.66044979A>T | GRCh37 |
| NC_000006.10:g.66101700A>T | NCBI36 |
| NG_023443.1:g.377140T>A | |
| NG_023443.2:g.377140T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000503581.6:c.1660T>A MANE Select | ENSP00000424243.1:p.Cys554Ser | |
| ENST00000342421.9:c.1660T>A | ENSP00000341818.5:p.Cys554Ser | |
| ENST00000370616.6:c.1660T>A | ENSP00000359650.2:p.Cys554Ser | |
| ENST00000370618.7:c.1660T>A | ENSP00000359652.4:p.Cys554Ser | |
| ENST00000370621.7:c.1660T>A | ENSP00000359655.3:p.Cys554Ser | |
| ENST00000393380.6:c.1660T>A | ENSP00000377042.2:p.Cys554Ser | |
| ENST00000503581.5:c.1660T>A | ENSP00000424243.1:p.Cys554Ser | |
| NM_001142800.1:c.1660T>A | NP_001136272.1:p.Cys554Ser | |
| NM_001142801.1:c.1660T>A | NP_001136273.1:p.Cys554Ser | |
| NM_001292009.1:c.1660T>A | NP_001278938.1:p.Cys554Ser | |
| NM_198283.1:c.1660T>A | NP_938024.1:p.Cys554Ser | |
| NM_001142800.2:c.1660T>A MANE Select | NP_001136272.1:p.Cys554Ser | |
| NM_001142801.2:c.1660T>A | NP_001136273.1:p.Cys554Ser | |
| NM_001292009.2:c.1660T>A | NP_001278938.1:p.Cys554Ser | |
| NM_198283.2:c.1660T>A | NP_938024.1:p.Cys554Ser |