Linked Data
dbSNP Id:
rs749082163
ExAC:
1:17674469 C / T
gnomAD v2:
1-17674469-C-T
gnomAD v3:
1-17347974-C-T
gnomAD v4:
1-17347974-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.17347974C>T , CM000663.2:g.17347974C>T | GRCh38 |
| NC_000001.10:g.17674469C>T , CM000663.1:g.17674469C>T | GRCh37 |
| NC_000001.9:g.17547056C>T | NCBI36 |
| NG_023261.2:g.44785C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375448.4:c.1081C>T MANE Select | ENSP00000364597.4:p.His361Tyr | |
| ENST00000468945.1:n.140C>T | ||
| ENST00000487048.5:n.48C>T | ||
| NM_012387.2:c.1081C>T | NP_036519.2:p.His361Tyr | |
| XM_011541150.1:c.895C>T | XP_011539452.1:p.His299Tyr | |
| XM_011541151.1:c.1081C>T | XP_011539453.1:p.His361Tyr | |
| XM_011541152.1:c.544C>T | XP_011539454.1:p.His182Tyr | |
| XM_011541153.1:c.1081C>T | XP_011539455.1:p.His361Tyr | |
| XM_011541154.1:c.1081C>T | XP_011539456.1:p.His361Tyr | |
| XM_011541155.1:c.1081C>T | XP_011539457.1:p.His361Tyr | |
| XM_011541156.1:c.1081C>T | XP_011539458.1:p.His361Tyr | |
| XM_011541157.1:c.190C>T | XP_011539459.1:p.His64Tyr | |
| XM_011541154.2:c.1081C>T | XP_011539456.1:p.His361Tyr | |
| NM_012387.3:c.1081C>T MANE Select | NP_036519.2:p.His361Tyr |