HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55154839G= , CM000681.2:g.55154839G= | GRCh38 |
NC_000019.9:g.55666207G= , CM000681.1:g.55666207G= | GRCh37 |
NC_000019.8:g.60358019G= | NCBI36 |
NG_007866.2:g.7894C= , LRG_432:g.7894C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344887.10:c.283-9C= MANE Select | ENSP00000341838.5:n.283-9C= | |
ENST00000665070.1:c.283-9C= | ENSP00000499482.1:n.283-9C= | |
ENST00000344887.9:c.283-9C= | ENSP00000341838.5:n.283-9C= | |
ENST00000585806.5:n.282-9C= | ||
ENST00000586669.5:n.291-9C= | ||
ENST00000587176.5:n.467-9C= | ||
ENST00000587871.1:c.902-9C= | ||
ENST00000588882.1:c.208-9C= | ENSP00000466729.1:n.208-9C= | |
ENST00000590463.1:n.455-9C= | ||
NM_000363.4:c.283-9C= , LRG_432t1:c.283-9C= | NP_000354.4:n.283-9C= | |
NM_000363.5:c.283-9C= MANE Select | NP_000354.4:n.283-9C= |