Linked Data
ClinVar Variation Id:
1631294
dbSNP Id:
rs138858983
ExAC:
1:12317052 C / T
gnomAD v2:
1-12317052-C-T
gnomAD v3:
1-12256995-C-T
gnomAD v4:
1-12256995-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.12256995C>T , CM000663.2:g.12256995C>T | GRCh38 |
| NC_000001.10:g.12317052C>T , CM000663.1:g.12317052C>T | GRCh37 |
| NC_000001.9:g.12239639C>T | NCBI36 |
| NG_056877.1:g.31957C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000620676.6:c.849C>T MANE Select | ENSP00000478104.1:p.Tyr283= | |
| ENST00000489961.1:n.330C>T | ||
| ENST00000613099.4:c.849C>T | ENSP00000482233.1:p.Tyr283= | |
| ENST00000620676.4:c.849C>T | ENSP00000478104.1:p.Tyr283= | |
| NM_015378.3:c.849C>T | NP_056193.2:p.Tyr283= | |
| NM_018156.3:c.849C>T | NP_060626.2:p.Tyr283= | |
| NM_015378.4:c.849C>T MANE Select | NP_056193.2:p.Tyr283= | |
| NM_018156.4:c.849C>T | NP_060626.2:p.Tyr283= |