HGVS | Genome Assembly |
---|---|
NC_000019.10:g.7528304G= , CM000681.2:g.7528304G= | GRCh38 |
NC_000019.9:g.7593190G= , CM000681.1:g.7593190G= | GRCh37 |
NC_000019.8:g.7499190G= | NCBI36 |
NG_015806.1:g.10695G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264079.11:c.877+47G= MANE Select | ENSP00000264079.5:n.877+47G= | |
ENST00000264079.10:c.877+47G= | ENSP00000264079.5:n.877+47G= | |
ENST00000394321.9:n.1192+47G= | ||
NM_020533.2:c.877+47G= | NP_065394.1:n.877+47G= | |
NM_020533.3:c.877+47G= MANE Select | NP_065394.1:n.877+47G= |