HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94060596A= , CM000663.2:g.94060596A= | GRCh38 |
NC_000001.10:g.94526152A= , CM000663.1:g.94526152A= | GRCh37 |
NC_000001.9:g.94298740A= | NCBI36 |
NG_009073.1:g.65554T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.2101T= MANE Select | ENSP00000359245.3:p.Phe701= | |
ENST00000649773.1:c.2101T= | ENSP00000496882.1:p.Phe701= | |
ENST00000370225.3:c.2101T= | ENSP00000359245.3:p.Phe701= | |
ENST00000472033.1:n.221T= | ||
ENST00000536513.5:c.-65+2578T= | ENSP00000439707.2:n.-65+2578T= | |
NM_000350.2:c.2101T= | NP_000341.2:p.Phe701= | |
NM_000350.3:c.2101T= MANE Select | NP_000341.2:p.Phe701= |