Linked Data
dbSNP Id:
rs1704764168
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.81646437T>G , CM000665.2:g.81646437T>G | GRCh38 |
| NC_000003.11:g.81695588T>G , CM000665.1:g.81695588T>G | GRCh37 |
| NC_000003.10:g.81778278T>G | NCBI36 |
| NG_011810.1:g.120364A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000429644.7:c.737A>C MANE Select | ENSP00000410833.2:p.Tyr246Ser | |
| ENST00000429644.6:c.737A>C | ENSP00000410833.2:p.Tyr246Ser | |
| ENST00000489715.1:c.614A>C | ENSP00000419638.1:p.Tyr205Ser | |
| ENST00000498468.1:n.287A>C | ||
| NM_000158.3:c.737A>C | NP_000149.3:p.Tyr246Ser | |
| NM_000158.4:c.737A>C MANE Select | NP_000149.4:p.Tyr246Ser |