HGVS | Genome Assembly |
---|---|
NC_000023.11:g.47588458G>C , CM000685.2:g.47588458G>C | GRCh38 |
NC_000023.10:g.47447857G>C , CM000685.1:g.47447857G>C | GRCh37 |
NC_000023.9:g.47332801G>C | NCBI36 |
NG_008437.1:g.36400C>G | |
NG_012533.1:g.11168G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000295987.13:c.775-10957C>G MANE Select | ENSP00000295987.7:n.775-10957C>G | |
ENST00000340666.5:c.775-10957C>G | ENSP00000343206.4:n.775-10957C>G | |
ENST00000295987.11:c.775-10957C>G | ENSP00000295987.7:n.775-10957C>G | |
ENST00000340666.4:c.775-10957C>G | ENSP00000343206.4:n.775-10957C>G | |
NM_006950.3:c.775-10957C>G MANE Select | NP_008881.2:n.775-10957C>G | |
NM_133499.2:c.775-10957C>G | NP_598006.1:n.775-10957C>G |