HGVS | Genome Assembly |
---|---|
NC_000008.11:g.1296051T>G , CM000670.2:g.1296051T>G | GRCh38 |
NC_000008.10:g.1244311T>G , CM000670.1:g.1244311T>G | GRCh37 |
NC_000008.9:g.1231718T>G | NCBI36 |
NG_009409.2:g.563333T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000421627.7:c.103+37168T>G | ENSP00000400258.3:n.103+37168T>G | |
ENST00000637795.2:c.106+37168T>G MANE Select | ENSP00000489774.1:n.106+37168T>G | |
NR_111948.1:n.3032A>C | ||
XM_011534761.1:c.-135+37168T>G | XP_011533063.1:n.-135+37168T>G | |
XM_011534762.1:c.-135+37168T>G | XP_011533064.1:n.-135+37168T>G | |
NM_001346810.1:c.106+37168T>G | NP_001333739.1:n.106+37168T>G | |
NM_001346810.2:c.106+37168T>G MANE Select | NP_001333739.1:n.106+37168T>G |