HGVS | Genome Assembly |
---|---|
NC_000018.10:g.69615742A= , CM000680.2:g.69615742A= | GRCh38 |
NC_000018.9:g.67282978A= , CM000680.1:g.67282978A= | GRCh37 |
NC_000018.8:g.65433958A= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382713.10:c.289+16244A= MANE Select | ENSP00000372160.5:n.289+16244A= | |
ENST00000382713.9:c.289+16244A= | ENSP00000372160.5:n.289+16244A= | |
NM_152721.5:c.289+16244A= | NP_689934.2:n.289+16244A= | |
XM_011525873.1:c.289+16244A= | XP_011524175.1:n.289+16244A= | |
XM_011525874.1:c.289+16244A= | XP_011524176.1:n.289+16244A= | |
XM_011525875.1:c.289+16244A= | XP_011524177.1:n.289+16244A= | |
XM_011525875.2:c.289+16244A= | XP_011524177.1:n.289+16244A= | |
NM_152721.6:c.289+16244A= MANE Select | NP_689934.2:n.289+16244A= |