HGVS | Genome Assembly |
---|---|
NC_000014.9:g.96204915T= , CM000676.2:g.96204915T= | GRCh38 |
NC_000014.8:g.96671252T= , CM000676.1:g.96671252T= | GRCh37 |
NC_000014.7:g.95741005T= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000554311.2:c.-84T= MANE Select | ENSP00000450482.1:n.-84T= | |
ENST00000539359.1:c.-326T= | ENSP00000438376.1:n.-326T= | |
ENST00000542454.2:c.-2852T= | ENSP00000439459.2:n.-2852T= | |
ENST00000553811.1:c.-79T= | ENSP00000450984.1:n.-79T= | |
ENST00000554311.1:c.-84T= | ENSP00000450482.1:n.-84T= | |
NM_000623.3:c.-79T= | NP_000614.1:n.-79T= | |
NM_000623.4:c.-79T= | NP_000614.1:n.-79T= | |
NM_001379692.1:c.-84T= MANE Select | NP_001366621.1:n.-84T= |