HGVS | Genome Assembly |
---|---|
NC_000011.10:g.118312704A= , CM000673.2:g.118312704A= | GRCh38 |
NC_000011.9:g.118183419A= , CM000673.1:g.118183419A= | GRCh37 |
NC_000011.8:g.117688629A= | NCBI36 |
NG_007383.1:g.13125A= , LRG_38:g.13125A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361763.9:c.190A= MANE Select | ENSP00000354566.4:p.Lys64= | |
ENST00000361763.8:c.190A= | ENSP00000354566.4:p.Lys64= | |
ENST00000526146.5:n.736A= | ||
ENST00000528435.5:n.743A= | ||
ENST00000528600.1:c.172A= | ENSP00000433975.1:p.Lys58= | |
ENST00000529713.5:n.296A= | ||
ENST00000531913.1:n.561A= | ||
NM_000733.3:c.190A= , LRG_38t1:c.190A= | NP_000724.1:p.Lys64= | |
NM_000733.4:c.190A= MANE Select | NP_000724.1:p.Lys64= |