HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240875242G= , CM000664.2:g.240875242G= | GRCh38 |
NC_000002.11:g.241814659G= , CM000664.1:g.241814659G= | GRCh37 |
NC_000002.10:g.241463332G= | NCBI36 |
NG_008005.1:g.11498G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307503.4:c.776+38G= MANE Select | ENSP00000302620.3:n.776+38G= | |
ENST00000307503.3:c.776+38G= | ENSP00000302620.3:n.776+38G= | |
ENST00000476698.1:n.428+38G= | ||
NM_000030.2:c.776+38G= | NP_000021.1:n.776+38G= | |
NM_000030.3:c.776+38G= MANE Select | NP_000021.1:n.776+38G= |