HGVS | Genome Assembly |
---|---|
NC_000019.10:g.3926031C= , CM000681.2:g.3926031C= | GRCh38 |
NC_000019.9:g.3926029C= , CM000681.1:g.3926029C= | GRCh37 |
NC_000019.8:g.3877029C= | NCBI36 |
NG_012638.1:g.50412C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000450849.7:c.*1439C= MANE Select | ENSP00000390941.1:n.*1439C= | |
ENST00000450849.6:c.*1439C= | ENSP00000390941.1:n.*1439C= | |
ENST00000600960.1:c.2619C= | ENSP00000470842.1:n.2619C= | |
ENST00000601323.1:n.440-227C= | ||
NM_033064.4:c.*1439C= | NP_149053.1:n.*1439C= | |
NM_033064.5:c.*1439C= MANE Select | NP_149053.1:n.*1439C= |