Linked Data
ClinVar Variation Id:
240979
dbSNP Id:
rs142278066
ExAC:
2:73826621 C / T
gnomAD v2:
2-73826621-C-T
gnomAD v3:
2-73599494-C-T
gnomAD v4:
2-73599494-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.73599494C>T , CM000664.2:g.73599494C>T | GRCh38 |
| NC_000002.11:g.73826621C>T , CM000664.1:g.73826621C>T | GRCh37 |
| NC_000002.10:g.73680129C>T | NCBI36 |
| NG_011690.1:g.218742C>T , LRG_741:g.218742C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682565.1:c.11260C>T | ENSP00000507671.1:p.His3754Tyr | |
| ENST00000682801.1:c.11167-2691C>T | ENSP00000507862.1:n.11167-2691C>T | |
| ENST00000682859.1:c.11260C>T | ENSP00000508222.1:p.His3754Tyr | |
| ENST00000683791.1:c.4346C>T | ||
| ENST00000684460.1:c.8541C>T | ||
| ENST00000684548.1:c.11260C>T | ENSP00000507421.1:p.His3754Tyr | |
| ENST00000684590.1:c.5707C>T | ENSP00000507376.1:p.His1903Tyr | |
| ENST00000684656.1:c.8725C>T | ||
| ENST00000613296.6:c.11641C>T MANE Select | ENSP00000482968.1:p.His3881Tyr | |
| ENST00000651057.1:c.1795C>T | ENSP00000498504.1:p.His599Tyr | |
| ENST00000651434.1:c.2997C>T | ||
| ENST00000651750.1:c.1029C>T | ||
| ENST00000652487.1:c.2812C>T | ||
| ENST00000484298.5:c.11515C>T | ENSP00000478155.1:p.His3839Tyr | |
| ENST00000613296.4:c.11641C>T | ENSP00000482968.1:p.His3881Tyr | |
| ENST00000620466.4:n.5444C>T | ||
| NM_015120.4:c.11644C>T , LRG_741t1:c.11644C>T | NP_055935.4:p.His3882Tyr | |
| NM_001378454.1:c.11641C>T MANE Select | NP_001365383.1:p.His3881Tyr |