HGVS | Genome Assembly |
---|---|
NC_000017.11:g.43755780G= , CM000679.2:g.43755780G= | GRCh38 |
NC_000017.10:g.41833148G= , CM000679.1:g.41833148G= | GRCh37 |
NC_000017.9:g.39188674G= | NCBI36 |
NG_008078.2:g.8009C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000301691.3:c.221-17C= MANE Select | ENSP00000301691.1:n.221-17C= | |
ENST00000301691.2:c.221-17C= | ENSP00000301691.1:n.221-17C= | |
NM_025237.2:c.221-17C= | NP_079513.1:n.221-17C= | |
NM_025237.3:c.221-17C= MANE Select | NP_079513.1:n.221-17C= |