HGVS | Genome Assembly |
---|---|
NC_000005.10:g.45462183A= , CM000667.2:g.45462183A= | GRCh38 |
NC_000005.9:g.45462285A= , CM000667.1:g.45462285A= | GRCh37 |
NC_000005.8:g.45498042A= | NCBI36 |
NG_042183.1:g.238936T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000303230.6:c.850-176T= MANE Select | ENSP00000307342.4:n.850-176T= | |
ENST00000637305.1:n.13-176T= | ||
ENST00000673735.1:c.850-176T= | ENSP00000501107.1:n.850-176T= | |
ENST00000303230.5:c.850-176T= | ENSP00000307342.4:n.850-176T= | |
NM_021072.3:c.850-176T= | NP_066550.2:n.850-176T= | |
NM_021072.4:c.850-176T= MANE Select | NP_066550.2:n.850-176T= |