HGVS | Genome Assembly |
---|---|
NC_000022.11:g.36564721A>G , CM000684.2:g.36564721A>G | GRCh38 |
NC_000022.10:g.36960768A>G , CM000684.1:g.36960768A>G | GRCh37 |
NC_000022.9:g.35290714A>G | NCBI36 |
NG_031861.1:g.142923T>C | |
NG_031861.2:g.143138T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000300105.7:c.602T>C MANE Select | ENSP00000300105.6:p.Phe201Ser | |
ENST00000300105.6:c.602T>C | ENSP00000300105.6:p.Phe201Ser | |
NM_006078.3:c.602T>C | NP_006069.1:p.Phe201Ser | |
NM_006078.4:c.602T>C | NP_006069.1:p.Phe201Ser | |
XM_017028531.2:c.344T>C | XP_016884020.1:p.Phe115Ser | |
NM_001379051.1:c.533T>C | NP_001365980.1:p.Phe178Ser | |
NM_006078.5:c.602T>C MANE Select | NP_006069.1:p.Phe201Ser | |
NR_166440.1:n.1968T>C |