HGVS | Genome Assembly |
---|---|
NC_000008.11:g.142914722T>G , CM000670.2:g.142914722T>G | GRCh38 |
NC_000008.10:g.143996138T>G , CM000670.1:g.143996138T>G | GRCh37 |
NC_000008.9:g.143993140T>G | NCBI36 |
NG_008374.1:g.8122A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000323110.2:c.782A>C (CYP11B2) MANE Select | ENSP00000325822.2:p.Asp261Ala | |
ENST00000522728.5:c.264+677T>G (GML) | ENSP00000430799.1:n.264+677T>G | |
NM_000498.3:c.782A>C (CYP11B2) MANE Select | NP_000489.3:p.Asp261Ala | |
XM_011516877.1:c.860A>C (CYP11B2) | XP_011515179.1:p.Asp287Ala | |
XM_011516878.1:c.860A>C (CYP11B2) | XP_011515180.1:p.Asp287Ala | |
XM_011516879.1:c.782A>C (CYP11B2) | XP_011515181.1:p.Asp261Ala | |
XM_011516970.1:c.297+677T>G (GML) | XP_011515272.1:n.297+677T>G |