HGVS | Genome Assembly |
---|---|
NC_000001.11:g.216418717T= , CM000663.2:g.216418717T= | GRCh38 |
NC_000001.10:g.216592059T= , CM000663.1:g.216592059T= | GRCh37 |
NC_000001.9:g.214658682T= | NCBI36 |
NG_009497.1:g.9680A= | |
NG_009497.2:g.9732A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307340.8:c.486-38A= MANE Select | ENSP00000305941.3:n.486-38A= | |
ENST00000674083.1:c.486-38A= | ENSP00000501296.1:n.486-38A= | |
ENST00000307340.7:c.486-38A= | ENSP00000305941.3:n.486-38A= | |
ENST00000366942.3:c.486-38A= | ENSP00000355909.3:n.486-38A= | |
NM_007123.5:c.486-38A= | NP_009054.5:n.486-38A= | |
NM_206933.2:c.486-38A= | NP_996816.2:n.486-38A= | |
NM_206933.3:c.486-38A= | NP_996816.2:n.486-38A= | |
NM_007123.6:c.486-38A= | NP_009054.6:n.486-38A= | |
NM_206933.4:c.486-38A= MANE Select | NP_996816.3:n.486-38A= |