HGVS | Genome Assembly |
---|---|
NC_000020.11:g.3857812G= , CM000682.2:g.3857812G= | GRCh38 |
NC_000020.10:g.3838459G= , CM000682.1:g.3838459G= | GRCh37 |
NC_000020.9:g.3786459G= | NCBI36 |
NG_030028.1:g.16014G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000428216.4:c.292+3G= MANE Select | ENSP00000401980.2:n.292+3G= | |
ENST00000416600.6:c.-132+3071G= | ENSP00000413749.2:n.-132+3071G= | |
ENST00000428216.3:c.292+3G= | ENSP00000401980.2:n.292+3G= | |
NM_001206491.1:c.-132+3071G= | NP_001193420.1:n.-132+3071G= | |
NM_020746.4:c.292+3G= | NP_065797.2:n.292+3G= | |
NR_037921.1:n.464+3G= | ||
NM_020746.5:c.292+3G= MANE Select | NP_065797.2:n.292+3G= | |
NR_037921.2:n.429+3G= | ||
NM_001206491.2:c.-132+3071G= | NP_001193420.1:n.-132+3071G= | |
NM_001385663.1:c.-256+3G= | NP_001372592.1:n.-256+3G= |