Linked Data
ClinVar Variation Id:
65873
dbSNP Id:
rs72551314
ExAC:
2:219676973 C / T
gnomAD v2:
2-219676973-C-T
gnomAD v3:
2-218812250-C-T
gnomAD v4:
2-218812250-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218812250C>T , CM000664.2:g.218812250C>T | GRCh38 |
| NC_000002.11:g.219676973C>T , CM000664.1:g.219676973C>T | GRCh37 |
| NC_000002.10:g.219385217C>T | NCBI36 |
| NG_007959.1:g.35502C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258415.9:c.475C>T MANE Select | ENSP00000258415.4:p.Gln159Ter | |
| ENST00000258415.8:c.475C>T | ENSP00000258415.4:p.Gln159Ter | |
| ENST00000411688.1:c.193C>T | ENSP00000392671.1:p.Gln65Ter | |
| ENST00000445971.1:c.284C>T | ENSP00000404945.1:p.Pro95Leu | |
| ENST00000466602.1:n.293C>T | ||
| ENST00000494263.5:n.909C>T | ||
| NM_000784.3:c.475C>T | NP_000775.1:p.Gln159Ter | |
| XM_017003488.2:c.55C>T | XP_016858977.1:p.Gln19Ter | |
| NM_000784.4:c.475C>T MANE Select | NP_000775.1:p.Gln159Ter |