HGVS | Genome Assembly |
---|---|
NC_000023.11:g.47588379T= , CM000685.2:g.47588379T= | GRCh38 |
NC_000023.10:g.47447778T= , CM000685.1:g.47447778T= | GRCh37 |
NC_000023.9:g.47332722T= | NCBI36 |
NG_008437.1:g.36479A= | |
NG_012533.1:g.11089T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000295987.13:c.775-10878A= MANE Select | ENSP00000295987.7:n.775-10878A= | |
ENST00000340666.5:c.775-10878A= | ENSP00000343206.4:n.775-10878A= | |
ENST00000295987.11:c.775-10878A= | ENSP00000295987.7:n.775-10878A= | |
ENST00000340666.4:c.775-10878A= | ENSP00000343206.4:n.775-10878A= | |
NM_006950.3:c.775-10878A= MANE Select | NP_008881.2:n.775-10878A= | |
NM_133499.2:c.775-10878A= | NP_598006.1:n.775-10878A= |