HGVS | Genome Assembly |
---|---|
NC_000001.11:g.55039717T= , CM000663.2:g.55039717T= | GRCh38 |
NC_000001.10:g.55505390T= , CM000663.1:g.55505390T= | GRCh37 |
NC_000001.9:g.55277978T= | NCBI36 |
NG_009061.1:g.5171T= , LRG_275:g.5171T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000673913.2:c.-121T= | ENSP00000501161.2:n.-121T= | |
ENST00000710286.1:c.237T= | ENSP00000518176.1:p.Pro79= | |
ENST00000673726.1:c.-121T= | ENSP00000501004.1:n.-121T= | |
ENST00000302118.5:c.-121T= MANE Select | ENSP00000303208.5:n.-121T= | |
NM_174936.3:c.-121T= , LRG_275t1:c.-121T= | NP_777596.2:n.-121T= | |
NM_174936.4:c.-121T= MANE Select | NP_777596.2:n.-121T= |