Linked Data
dbSNP Id:
rs1597064007
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.1985894A>G , CM000678.2:g.1985894A>G | GRCh38 |
| NC_000016.9:g.2035895A>G , CM000678.1:g.2035895A>G | GRCh37 |
| NC_000016.8:g.1975896A>G | NCBI36 |
| NG_016288.1:g.6746A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000567719.2:c.259A>G | ENSP00000455885.1:p.Thr87Ala | |
| ENST00000248114.7:c.484A>G MANE Select | ENSP00000248114.6:p.Thr162Ala | |
| ENST00000248114.6:c.484A>G | ENSP00000248114.6:p.Thr162Ala | |
| ENST00000565658.1:n.641A>G | ||
| ENST00000567719.1:c.259A>G | ENSP00000455885.1:p.Thr87Ala | |
| ENST00000569451.1:c.287A>G | ENSP00000456432.1:p.His96Arg | |
| NM_005262.2:c.484A>G | NP_005253.3:p.Thr162Ala | |
| NM_005262.3:c.484A>G MANE Select | NP_005253.3:p.Thr162Ala |