HGVS | Genome Assembly |
---|---|
NC_000016.10:g.1985820T= , CM000678.2:g.1985820T= | GRCh38 |
NC_000016.9:g.2035821T= , CM000678.1:g.2035821T= | GRCh37 |
NC_000016.8:g.1975822T= | NCBI36 |
NG_016288.1:g.6672T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000567719.2:c.231-46T= | ENSP00000455885.1:n.231-46T= | |
ENST00000248114.7:c.456-46T= MANE Select | ENSP00000248114.6:n.456-46T= | |
ENST00000248114.6:c.456-46T= | ENSP00000248114.6:n.456-46T= | |
ENST00000565658.1:n.613-46T= | ||
ENST00000567719.1:c.231-46T= | ENSP00000455885.1:n.231-46T= | |
ENST00000569451.1:c.259-46T= | ENSP00000456432.1:n.259-46T= | |
NM_005262.2:c.456-46T= | NP_005253.3:n.456-46T= | |
NM_005262.3:c.456-46T= MANE Select | NP_005253.3:n.456-46T= |