HGVS | Genome Assembly |
---|---|
NC_000005.10:g.154227888C>G , CM000667.2:g.154227888C>G | GRCh38 |
NC_000005.9:g.153607448C>G , CM000667.1:g.153607448C>G | GRCh37 |
NC_000005.8:g.153587641C>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000297107.11:c.159+36863C>G MANE Select | ENSP00000297107.6:n.159+36863C>G | |
ENST00000297107.10:c.159+36863C>G | ENSP00000297107.6:n.159+36863C>G | |
ENST00000377661.2:c.159+36863C>G | ENSP00000366889.2:n.159+36863C>G | |
ENST00000425427.6:c.159+36863C>G | ENSP00000415210.2:n.159+36863C>G | |
ENST00000520647.5:c.159+36863C>G | ENSP00000428573.1:n.159+36863C>G | |
ENST00000521781.5:n.150+9739C>G | ||
NM_198321.3:c.159+36863C>G | NP_938080.1:n.159+36863C>G | |
NM_198321.4:c.159+36863C>G MANE Select | NP_938080.1:n.159+36863C>G |