Linked Data
ClinVar Variation Id:
525414
ClinVar RCV Id:
RCV000629470
dbSNP Id:
rs751575627
ExAC:
7:21599339 C / T
gnomAD v2:
7-21599339-C-T
gnomAD v3:
7-21559721-C-T
gnomAD v4:
7-21559721-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.21559721C>T , CM000669.2:g.21559721C>T | GRCh38 |
| NC_000007.13:g.21599339C>T , CM000669.1:g.21599339C>T | GRCh37 |
| NC_000007.12:g.21565864C>T | NCBI36 |
| NG_012886.2:g.21507C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000409508.8:c.811C>T MANE Select | ENSP00000475939.1:p.His271Tyr | |
| ENST00000328843.10:c.811C>T | ENSP00000330671.7:p.His271Tyr | |
| ENST00000409508.7:c.811C>T | ENSP00000475939.1:p.His271Tyr | |
| ENST00000483691.1:n.7C>T | ||
| ENST00000620169.4:c.811C>T | ENSP00000481693.1:p.His271Tyr | |
| NM_001277115.1:c.811C>T | NP_001264044.1:p.His271Tyr | |
| NM_001277115.2:c.811C>T MANE Select | NP_001264044.1:p.His271Tyr |