Linked Data
ClinVar Variation Id:
2146805
ClinVar RCV Id:
RCV003067311
dbSNP Id:
rs770875542
ExAC:
17:42426853 C / T
gnomAD v2:
17-42426853-C-T
gnomAD v3:
17-44349485-C-T
gnomAD v4:
17-44349485-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.44349485C>T , CM000679.2:g.44349485C>T | GRCh38 |
| NC_000017.10:g.42426853C>T , CM000679.1:g.42426853C>T | GRCh37 |
| NC_000017.9:g.39782379C>T | NCBI36 |
| NG_007886.1:g.9363C>T , LRG_661:g.9363C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000053867.8:c.198C>T MANE Select | ENSP00000053867.2:p.His66= | |
| ENST00000639447.1:c.198C>T | ENSP00000492014.1:p.His66= | |
| ENST00000053867.7:c.198C>T | ENSP00000053867.2:p.His66= | |
| ENST00000586782.5:c.198C>T | ENSP00000468318.1:p.His66= | |
| ENST00000587387.5:c.198C>T | ENSP00000467431.1:p.His66= | |
| ENST00000587518.5:c.198C>T | ENSP00000465518.1:p.His66= | |
| ENST00000587958.1:n.234C>T | ||
| ENST00000588143.5:c.198C>T | ENSP00000465375.1:p.His66= | |
| ENST00000588170.5:n.294C>T | ||
| ENST00000588237.5:c.198C>T | ENSP00000466611.1:p.His66= | |
| ENST00000589265.5:c.198C>T | ENSP00000467616.1:p.His66= | |
| ENST00000589536.5:c.198C>T | ENSP00000466956.1:p.His66= | |
| ENST00000591740.5:c.198C>T | ENSP00000467022.1:p.His66= | |
| ENST00000592323.5:n.361C>T | ||
| ENST00000592783.5:c.198C>T | ENSP00000467870.1:p.His66= | |
| ENST00000593167.5:c.198C>T | ENSP00000466405.1:p.His66= | |
| NM_002087.3:c.198C>T | NP_002078.1:p.His66= | |
| XM_005257253.1:c.198C>T | XP_005257310.1:p.His66= | |
| XM_024450730.1:c.198C>T | XP_024306498.1:p.His66= | |
| NM_002087.4:c.198C>T MANE Select | NP_002078.1:p.His66= |