HGVS | Genome Assembly |
---|---|
NC_000011.10:g.72196182C= , CM000673.2:g.72196182C= | GRCh38 |
NC_000011.9:g.71907226C= , CM000673.1:g.71907226C= | GRCh37 |
NC_000011.8:g.71584874C= | NCBI36 |
NG_015863.1:g.11625C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000312293.9:c.*5C= | ENSP00000308137.4:n.*5C= | |
ENST00000393676.5:c.*5C= MANE Select | ENSP00000377281.3:n.*5C= | |
ENST00000675784.1:c.*5C= | ENSP00000502440.1:n.*5C= | |
ENST00000312293.8:c.*5C= | ENSP00000308137.4:n.*5C= | |
ENST00000393676.3:c.*5C= | ENSP00000377281.3:n.*5C= | |
ENST00000393679.5:c.*5C= | ENSP00000377284.1:n.*5C= | |
ENST00000393681.6:c.*5C= | ENSP00000377286.2:n.*5C= | |
NM_000802.3:c.*5C= | NP_000793.1:n.*5C= | |
NM_016724.2:c.*5C= | NP_057936.1:n.*5C= | |
NM_016725.2:c.*5C= | NP_057937.1:n.*5C= | |
NM_016729.2:c.*5C= | NP_057941.1:n.*5C= | |
NM_016729.3:c.*5C= MANE Select | NP_057941.1:n.*5C= | |
NM_016724.3:c.*5C= | NP_057936.1:n.*5C= | |
NM_016725.3:c.*5C= | NP_057937.1:n.*5C= |