HGVS | Genome Assembly |
---|---|
NC_000003.12:g.138946166T>G , CM000665.2:g.138946166T>G | GRCh38 |
NC_000003.11:g.138665008T>G , CM000665.1:g.138665008T>G | GRCh37 |
NC_000003.10:g.140147698T>G | NCBI36 |
NG_012454.1:g.5975A>C | |
NG_029796.1:g.3933T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000648323.1:c.557A>C MANE Select | ENSP00000497217.1:p.Tyr186Ser | |
ENST00000330315.3:c.557A>C | ENSP00000333188.3:p.Tyr186Ser | |
NM_023067.3:c.557A>C | NP_075555.1:p.Tyr186Ser | |
NM_023067.4:c.557A>C MANE Select | NP_075555.1:p.Tyr186Ser |