HGVS | Genome Assembly |
---|---|
NC_000014.9:g.96204911G= , CM000676.2:g.96204911G= | GRCh38 |
NC_000014.8:g.96671248G= , CM000676.1:g.96671248G= | GRCh37 |
NC_000014.7:g.95741001G= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000554311.2:c.-88G= MANE Select | ENSP00000450482.1:n.-88G= | |
ENST00000539359.1:c.-330G= | ENSP00000438376.1:n.-330G= | |
ENST00000542454.2:c.-2856G= | ENSP00000439459.2:n.-2856G= | |
ENST00000553811.1:c.-83G= | ENSP00000450984.1:n.-83G= | |
ENST00000554311.1:c.-88G= | ENSP00000450482.1:n.-88G= | |
NM_000623.3:c.-83G= | NP_000614.1:n.-83G= | |
NM_000623.4:c.-83G= | NP_000614.1:n.-83G= | |
NM_001379692.1:c.-88G= MANE Select | NP_001366621.1:n.-88G= |