Linked Data
ClinVar Variation Id:
377897
dbSNP Id:
rs202190197
ExAC:
17:41053025 C / T
gnomAD v2:
17-41053025-C-T
gnomAD v3:
17-42901008-C-T
gnomAD v4:
17-42901008-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42901008C>T , CM000679.2:g.42901008C>T | GRCh38 |
| NC_000017.10:g.41053025C>T , CM000679.1:g.41053025C>T | GRCh37 |
| NC_000017.9:g.38306551C>T | NCBI36 |
| NG_011808.1:g.5211C>T , LRG_147:g.5211C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253801.7:c.132C>T MANE Select | ENSP00000253801.1:p.Tyr44= | |
| ENST00000253801.6:c.132C>T | ENSP00000253801.1:p.Tyr44= | |
| ENST00000585489.1:c.132C>T | ENSP00000466202.1:p.Tyr44= | |
| ENST00000588481.1:n.197C>T | ||
| ENST00000592383.5:c.132C>T | ENSP00000465958.1:p.Tyr44= | |
| NM_000151.3:c.132C>T | NP_000142.2:p.Tyr44= | |
| NM_001270397.1:c.132C>T | NP_001257326.1:p.Tyr44= | |
| NM_000151.4:c.132C>T MANE Select | NP_000142.2:p.Tyr44= | |
| NM_001270397.2:c.132C>T | NP_001257326.1:p.Tyr44= |