HGVS | Genome Assembly |
---|---|
NC_000011.10:g.299478A>G , CM000673.2:g.299478A>G | GRCh38 |
NC_000011.9:g.299478A>G , CM000673.1:g.299478A>G | GRCh37 |
NC_000011.8:g.289478A>G | NCBI36 |
NG_032892.1:g.5049T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382614.2:c.13T>C MANE Select | ENSP00000372059.2:p.Tyr5His | |
NM_001025295.2:c.13T>C | NP_001020466.1:p.Tyr5His | |
NM_001025295.3:c.13T>C MANE Select | NP_001020466.1:p.Tyr5His |