HGVS | Genome Assembly |
---|---|
NC_000016.10:g.1986057G= , CM000678.2:g.1986057G= | GRCh38 |
NC_000016.9:g.2036058G= , CM000678.1:g.2036058G= | GRCh37 |
NC_000016.8:g.1976059G= | NCBI36 |
NG_016288.1:g.6909G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000567719.2:c.*29G= | ENSP00000455885.1:n.*29G= | |
ENST00000248114.7:c.*29G= MANE Select | ENSP00000248114.6:n.*29G= | |
ENST00000248114.6:c.*29G= | ENSP00000248114.6:n.*29G= | |
ENST00000565658.1:n.804G= | ||
ENST00000567719.1:c.*29G= | ENSP00000455885.1:n.*29G= | |
ENST00000569451.1:c.*120G= | ENSP00000456432.1:n.*120G= | |
NM_005262.2:c.*29G= | NP_005253.3:n.*29G= | |
NM_005262.3:c.*29G= MANE Select | NP_005253.3:n.*29G= |