HGVS | Genome Assembly |
---|---|
NC_000014.9:g.96204953G= , CM000676.2:g.96204953G= | GRCh38 |
NC_000014.8:g.96671290G= , CM000676.1:g.96671290G= | GRCh37 |
NC_000014.7:g.95741043G= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000554311.2:c.-46G= MANE Select | ENSP00000450482.1:n.-46G= | |
ENST00000539359.1:c.-288G= | ENSP00000438376.1:n.-288G= | |
ENST00000542454.2:c.-2814G= | ENSP00000439459.2:n.-2814G= | |
ENST00000553811.1:c.-41G= | ENSP00000450984.1:n.-41G= | |
ENST00000554311.1:c.-46G= | ENSP00000450482.1:n.-46G= | |
NM_000623.3:c.-41G= | NP_000614.1:n.-41G= | |
NM_000623.4:c.-41G= | NP_000614.1:n.-41G= | |
NM_001379692.1:c.-46G= MANE Select | NP_001366621.1:n.-46G= |