Linked Data
dbSNP Id:
rs377172559
ExAC:
17:61566409 C / T
gnomAD v2:
17-61566409-C-T
gnomAD v3:
17-63489048-C-T
gnomAD v4:
17-63489048-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.63489048C>T , CM000679.2:g.63489048C>T | GRCh38 |
| NC_000017.10:g.61566409C>T , CM000679.1:g.61566409C>T | GRCh37 |
| NC_000017.9:g.58920141C>T | NCBI36 |
| NG_011648.1:g.16976C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000290866.10:c.2557C>T MANE Select | ENSP00000290866.4:p.His853Tyr | |
| ENST00000290863.10:c.835C>T | ENSP00000290863.6:p.His279Tyr | |
| ENST00000290866.9:c.2557C>T | ENSP00000290866.4:p.His853Tyr | |
| ENST00000413513.7:c.835C>T | ENSP00000392247.3:p.His279Tyr | |
| ENST00000428043.5:c.2557C>T | ENSP00000397593.2:p.His853Tyr | |
| ENST00000577647.2:c.835C>T | ENSP00000464149.1:p.His279Tyr | |
| ENST00000578839.5:c.*519+257C>T | ENSP00000462110.2:n.*519+257C>T | |
| ENST00000579314.5:c.*286C>T | ENSP00000462599.1:n.*286C>T | |
| ENST00000582005.5:c.*477C>T | ENSP00000462002.1:n.*477C>T | |
| ENST00000582761.1:c.325C>T | ENSP00000462909.1:p.His109Tyr | |
| ENST00000584865.5:n.503C>T | ||
| NM_000789.3:c.2557C>T | NP_000780.1:p.His853Tyr | |
| NM_001178057.1:c.835C>T | NP_001171528.1:p.His279Tyr | |
| NM_152830.2:c.835C>T | NP_690043.1:p.His279Tyr | |
| XM_005257110.1:c.2008C>T | XP_005257167.1:p.His670Tyr | |
| XM_006721737.2:c.895C>T | XP_006721800.2:p.His299Tyr | |
| XM_006721737.3:c.895C>T | XP_006721800.2:p.His299Tyr | |
| NM_000789.4:c.2557C>T MANE Select | NP_000780.1:p.His853Tyr | |
| NM_001178057.2:c.835C>T | NP_001171528.1:p.His279Tyr | |
| NM_152830.3:c.835C>T | NP_690043.1:p.His279Tyr | |
| NM_001382700.1:c.1990C>T | NP_001369629.1:p.His664Tyr | |
| NM_001382701.1:c.1705C>T | NP_001369630.1:p.His569Tyr | |
| NM_001382702.1:c.379+257C>T | NP_001369631.1:n.379+257C>T | |
| NR_168483.1:n.935C>T |