HGVS | Genome Assembly |
---|---|
NC_000011.10:g.118312695C= , CM000673.2:g.118312695C= | GRCh38 |
NC_000011.9:g.118183410C= , CM000673.1:g.118183410C= | GRCh37 |
NC_000011.8:g.117688620C= | NCBI36 |
NG_007383.1:g.13116C= , LRG_38:g.13116C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000361763.9:c.181C= MANE Select | ENSP00000354566.4:p.His61= | |
ENST00000361763.8:c.181C= | ENSP00000354566.4:p.His61= | |
ENST00000526146.5:n.727C= | ||
ENST00000528435.5:n.734C= | ||
ENST00000528600.1:c.163C= | ENSP00000433975.1:p.His55= | |
ENST00000529713.5:n.287C= | ||
ENST00000531913.1:n.552C= | ||
NM_000733.3:c.181C= , LRG_38t1:c.181C= | NP_000724.1:p.His61= | |
NM_000733.4:c.181C= MANE Select | NP_000724.1:p.His61= |