HGVS | Genome Assembly |
---|---|
NC_000022.11:g.27750488A= , CM000684.2:g.27750488A= | GRCh38 |
NC_000022.10:g.28146476A= , CM000684.1:g.28146476A= | GRCh37 |
NC_000022.9:g.26476476A= | NCBI36 |
NG_023258.1:g.56011T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000703102.1:n.915T= | ||
ENST00000302326.5:c.*427T= MANE Select | ENSP00000304956.4:n.*427T= | |
ENST00000302326.4:c.*427T= | ENSP00000304956.4:n.*427T= | |
ENST00000424656.1:c.456-260T= | ||
NM_002430.2:c.*427T= | NP_002421.3:n.*427T= | |
NM_002430.3:c.*427T= MANE Select | NP_002421.3:n.*427T= |