HGVS | Genome Assembly |
---|---|
NC_000019.10:g.1104036C= , CM000681.2:g.1104036C= | GRCh38 |
NC_000019.9:g.1104035C= , CM000681.1:g.1104035C= | GRCh37 |
NC_000019.8:g.1055035C= | NCBI36 |
NG_050621.1:g.5111C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706713.1:c.-8C= | ENSP00000516510.1:n.-8C= | |
ENST00000354171.13:c.-8C= MANE Select | ENSP00000346103.7:n.-8C= | |
ENST00000589115.6:c.-8C= | ENSP00000466872.3:n.-8C= | |
ENST00000354171.12:c.-8C= | ENSP00000346103.7:n.-8C= | |
ENST00000589115.5:c.-8C= | ENSP00000466872.2:n.-8C= | |
ENST00000616066.4:c.-8C= | ENSP00000485000.1:n.-8C= | |
NM_001039847.2:c.-8C= | NP_001034936.1:n.-8C= | |
NM_002085.4:c.-8C= | NP_002076.2:n.-8C= | |
NM_001039847.3:c.-8C= | NP_001034936.1:n.-8C= | |
NM_002085.5:c.-8C= MANE Select | NP_002076.2:n.-8C= |