Linked Data
ClinVar Variation Id:
128343
dbSNP Id:
rs2760118
ExAC:
6:24503590 C / T
gnomAD v2:
6-24503590-C-T
gnomAD v3:
6-24503362-C-T
gnomAD v4:
6-24503362-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.24503362C>T , CM000668.2:g.24503362C>T | GRCh38 |
| NC_000006.11:g.24503590C>T , CM000668.1:g.24503590C>T | GRCh37 |
| NC_000006.10:g.24611569C>T | NCBI36 |
| NG_008161.1:g.13394C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000357578.8:c.538C>T MANE Select | ENSP00000350191.3:p.His180Tyr | |
| ENST00000672352.1:c.301C>T | ENSP00000500876.1:p.His101Tyr | |
| ENST00000672557.1:c.456C>T | ||
| ENST00000672652.1:c.459C>T | ||
| ENST00000675422.1:n.1298C>T | ||
| ENST00000348925.2:c.538C>T | ENSP00000314649.3:p.His180Tyr | |
| ENST00000357578.7:c.538C>T | ENSP00000350191.3:p.His180Tyr | |
| ENST00000491546.5:c.454C>T | ENSP00000417687.1:p.His152Tyr | |
| NM_001080.3:c.538C>T MANE Select | NP_001071.1:p.His180Tyr | |
| NM_170740.1:c.538C>T | NP_733936.1:p.His180Tyr | |
| NM_001368954.1:c.538C>T | NP_001355883.1:p.His180Tyr |