HGVS | Genome Assembly |
---|---|
NC_000001.11:g.55039825T= , CM000663.2:g.55039825T= | GRCh38 |
NC_000001.10:g.55505498T= , CM000663.1:g.55505498T= | GRCh37 |
NC_000001.9:g.55278086T= | NCBI36 |
NG_009061.1:g.5279T= , LRG_275:g.5279T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000673913.2:c.-13T= | ENSP00000501161.2:n.-13T= | |
ENST00000710286.1:c.345T= | ENSP00000518176.1:p.Ser115= | |
ENST00000673726.1:c.-13T= | ENSP00000501004.1:n.-13T= | |
ENST00000302118.5:c.-13T= MANE Select | ENSP00000303208.5:n.-13T= | |
NM_174936.3:c.-13T= , LRG_275t1:c.-13T= | NP_777596.2:n.-13T= | |
NM_174936.4:c.-13T= MANE Select | NP_777596.2:n.-13T= |