Linked Data
dbSNP Id:
rs1703671092
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.81577966A>G , CM000665.2:g.81577966A>G | GRCh38 |
| NC_000003.11:g.81627117A>G , CM000665.1:g.81627117A>G | GRCh37 |
| NC_000003.10:g.81709807A>G | NCBI36 |
| NG_011810.1:g.188835T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000429644.7:c.1577T>C MANE Select | ENSP00000410833.2:p.Ile526Thr | |
| ENST00000429644.6:c.1577T>C | ENSP00000410833.2:p.Ile526Thr | |
| ENST00000489715.1:c.1454T>C | ENSP00000419638.1:p.Ile485Thr | |
| NM_000158.3:c.1577T>C | NP_000149.3:p.Ile526Thr | |
| NM_000158.4:c.1577T>C MANE Select | NP_000149.4:p.Ile526Thr |